Pediatric glossary of terms expanded: Difference between revisions
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Revision as of 22:16, 23 March 2025
Pediatric glossary of terms | Glossary of medical terms | Dictionary of pediatrics
- 10p13-p14 deletion syndrome
- 11 beta-hydroxysteroid dehydrogenase type 2 deficiency
- 11-beta-hydroxylase deficiency
- 11-beta-hydroxysteroid dehydrogenase type 1 deficiency
- 17-alpha-hydroxylase/17,20 lyase deficiency
- 17-beta-hydroxysteroid dehydrogenase 3 deficiency
- 21-hydroxylase deficiency
- 22q deletion syndrome(s)
- 3-beta-hydroxysteroid dehydrogenase deficiency
- 3-methylglutaconic aciduria type 1
- 45,x/46,xy gonadal dysgenesis
- 46,xx differences of sex development
- 46,xx gonadal dysgenesis
- 46,xx ovotesticular difference of sex development
- 46,xx testicular differences of sex development
- 46,xx/46,xy ovotesticular differences of sex development
- 46,xy differences of sex development
- 46,xy disorder of androgen action
- 46,xy gonadal dysgenesis
- 46,xy ovotesticular differences of sex development
- 47,xxx syndrome
- 47,xyy syndrome
- 5 alpha steroid reductase 2 deficiency
- 5,10-methylenetetrahydrofolate reductase deficiency
- 5-alpha-reductase deficiency
- A1 hydronephrosis
- A2/3 hydronephrosis
- Aarskog syndrome
- Abdominal aorta thrombosis
- Abdominal distention
- Abdominal migraine
- Abdominal pain
- Abdominal pregnancy
- Abnormal behavior
- Abnormal liver function test
- Abo hemolytic disease of newborn
- Abortion
- Abrasion
- Abscess
- Absence of bowel movement
- Absent baseline variability
- Absent physiologic conversion of uteroplacental vessel
- Abusive head trauma
- Acampomelic campomelic dysplasia (aq)
- Acanthosis nigricans
- Accelerated growth
- Accelerated placental villous maturation
- Accidental medicine ingestion
- Ace inhibitor
- Achondroplasia
- Acid-labile subunit deficiency
- Acne
- Acoria
- Acquired adrenocorticotropic hormone deficiency
- Acquired bilateral cataracts
- Acquired cataract
- Acquired central hypothyroidism
- Acquired chylothorax
- Acquired coagulation factor deficiency
- Acquired color blindness
- Acquired cytomegaloviral infection
- Acquired facial nerve palsy
- Acquired factor I deficiency
- Acquired factor ii deficiency
- Acquired factor iii deficiency
- Acquired factor ix deficiency
- Acquired factor v deficiency
- Acquired factor vii deficiency
- Acquired factor viii deficiency
- Acquired factor x deficiency
- Acquired factor xi deficiency
- Acquired factor xii deficiency
- Acquired factor xiii deficiency
- Acquired generalized lipodystrophy
- Acquired growth hormone deficiency
- Acquired hemolytic anemia
- Acquired hydrocephalus
- Acquired hyperthyroidism
- Acquired hypogonadotropic hypogonadism
- Acquired hypoparathyroidism
- Acquired hypothyroidism
- Acquired ichthyosis
- Acquired immunodeficiency disease
- Acquired methemoglobinemia
- Acquired neurogenic bladder
- Acquired ovarian failure
- Acquired partial lipodystrophy
- Acquired phrenic nerve injury
- Acquired phrenic nerve palsy
- Acquired pure red cell aplasia
- Acquired rickets
- Acquired solitary kidney
- Acquired testicular failure
- Acquired thrombotic thrombocytopenic purpura
- Acquired unilateral cataract
- Acquired urinary tract obstruction
- Acral erythema
- Acrocephalosyndactyly
- Acromegaly
- Acth-producing pituitary adenoma
- Activating thyroid stimulating hormone receptor gene mutation
- Active phase of labor
- Acute anterior uveitis
- Acute basophilic leukemia
- Acute bilineal leukemia
- Acute biphenotypic leukemia
- Acute cellular kidney allograft nephropathy
- Acute cortical necrosis
- Acute disseminated encephalomyelitis
- Acute erythroid leukemia
- Acute flaccid myelitis
- Acute generalized exanthematous pustulosis
- Acute glomerulonephritis
- Acute graft versus host disease
- Acute hemorrhagic edema of infancy
- Acute humoral kidney allograft nephropathy
- Acute inflammatory demyelinating polyradiculoneuropathy
- Acute intervillous thrombus
- Acute intrapartum hypoxic event
- Acute kidney allograft nephropathy
- Acute kidney injury
- Acute leukemia of ambiguous lineage
- Acute liver failure
- Acute lymphoblastic leukemia
- Acute megakaryoblastic leukemia
- Acute monoblastic and monocytic leukemia
- Acute motor and sensory axonal neuropathy
- Acute motor axonal neuropathy
- Acute myeloid leukemia occurring in children with down syndrome
- Acute myeloid leukemia with a variant rara translocation
- Acute myeloid leukemia with maturation
- Acute myeloid leukemia with minimal differentiation
- Acute myeloid leukemia with mutated cebpa
- Acute myeloid leukemia with mutated npm1
- Acute myeloid leukemia with myelodysplasia-related changes
- Acute myeloid leukemia with recurrent genetic abnormalities
- Acute myeloid leukemia with t(11;15)(p15;q35); nup98-jarid1a
- Acute myeloid leukemia with t(11;17)(q13;q21)
- Acute myeloid leukemia with t(11;17)(q23;q21)
- Acute myeloid leukemia with t(17;17)(q21;q21)
- Acute myeloid leukemia with t(5;11)(q35;p15); nup98-nsd1
- Acute myeloid leukemia with t(5;17)(q35;q21)
- Acute myeloid leukemia with t(6;9)(p23;q34); dek-nup214
- Acute myeloid leukemia with t(7;12)(q36;p13); hlxb9-etv6
- Acute myeloid leukemia with t(8;21)(q22;q22); runx1-runx1t1
- Acute myeloid leukemia with t(9;11)(p22;q23); mllt3-mll
- Acute myeloid leukemia with variant mll translocations
- Acute myeloid leukemia without maturation
- Acute myeloid leukemia
- Acute myelomonocytic leukemia
- Acute otitis media
- Acute placental infarct
- Acute poliomyelitis
- Acute promyelocytic leukemia with t(15;17)(q22;q12); pml-rara
- Acute pyelonephritis
- Acute respiratory failure
- Acute sinusitis
- Acute stress disorder
- Acute suppurative thyroiditis
- Acute transverse myelitis
- Acute tubular necrosis
- Acute undifferentiated leukemia
- Acute uric acid nephropathy
- Addison disease
- Address
- Adenovirus infection
- Adipose tissue deposition
- Adipsic diabetes insipidus
- Adolescence
- Adrenal androgen deficiency
- Adrenal androgen excess
- Adrenal crisis
- Adrenal hemorrhage
- Adrenal hypoplasia congenita
- Adrenal insufficiency
- Adrenocorticotropic hormone deficiency
- Adrenoleukodystrophy
- Adult intestinal botulism
- Advertise on WikiMD
- African trypanosomiasis
- Agalactia
- Ageusia
- Aggression
- Agitation
- Agonal respiration
- Agoraphobia
- Agranulocytosis
- Air embolism
- Airborne transmission
- Airway compromise
- Airway hemangioma
- Akathisia
- Akinesia
- Alagille syndrome
- Albinism
- Albright hereditary osteodystrophy with multiple hormone resistance
- Albright hereditary osteodystrophy
- Alcohol use history
- Aldosterone deficiency
- Aldosterone synthase deficiency type 1
- Aldosterone synthase deficiency type 2
- Aldosterone synthase deficiency
- Alice in wonderland syndrome
- Allantoic cyst
- Allergen
- Allergic bronchopulmonary aspergillosis
- Allergic reaction
- Allergic rhinitis
- Allis clamp fetal scalp stimulation
- Allogeneic
- Alloimmunization
- Alopecia
- Alpers disease
- Alpha fetoprotein increased
- Alpha thalassemia silent carrier
- Alpha thalassemia trait
- Alpha thalassemia
- Alpha-1-antitrypsin deficiency
- Alpha-beta t-cell depletion
- Alpha-fetoprotein measurement
- Alport syndrome
- Alström syndrome
- Altered level of consciousness
- Altered mental status
- Alveolar capillary dysplasia
- Amastia
- Amaurosis fugax
- Amblyopia
- Ambulation difficulty
- Amebiasis
- Amelia
- Amenorrhea
- American college of rheumatology classification criteria for juvenile rheumatoid arthritis
- American college of rheumatology classification criteria for systemic lupus erythematosus
- Amino acid measurement
- Amino acid metabolism disorder
- Amnesia
- Amniocentesis
- Amnion epithelium necrosis
- Amnion nodosum
- Amniotic band syndrome
- Amniotic fluid embolism
- Amotivation
- Anaphylaxis
- Anaplasmosis
- Anaplastic embryonal rhabdomyosarcoma
- Anaplastic thyroid carcinoma
- Anasarca
- Anatomic structure, system, or substance
- Androgen insensitivity syndrome
- Anemia due to decreased production
- Anemia due to disorder of glutathione metabolism
- Anemia due to disorder of nucleotide metabolism
- Anemia due to enzyme disorder
- Anemia due to erythrocyte enzyme disorder
- Anemia due to increased destruction
- Anemia of chronic disease
- Anemia of prematurity
- Anemia
- Anencephaly
- Anergy
- Anesthesia procedure
- Aneurysm
- Angelman syndrome
- Anger
- Angina
- Angioedema
- Angiomatosis
- Angiostrongyliasis
- Angiotensin converting enzyme inhibitor fetopathy
- Angiotensin ii receptor antagonist
- Angular cheilitis
- Anhedonia
- Anisakiasis
- Ankylosing spondylitis
- Annular lesion
- Annular pancreas
- Anophthalmos
- Anorexia nervosa
- Anorexia
- Anosmia
- Anovulation
- Anovulatory cycle
- Anoxia
- Antenatal hydronephrosis
- Antenatal steroids initiated
- Antepartum hemorrhage
- Antepartum obstetric air embolism
- Antepartum obstetric septic embolism
- Antepartum obstetric thromboembolism
- Antepartum stillbirth
- Antepartum uterine rupture
- Anterior segment ischemia
- Anterior uveitis
- Anthrax
- Anti-beta-2 glycoprotein 1 antibody
- Anti-convulsant hypersensitivity syndrome
- Anti-d hemolytic disease of the newborn
- Anti-ds dna antibody
- Anti-glomerular basement membrane antibody disease
- Anti-la antibody
- Anti-malarial agent
- Anti-ribonucleoprotein antibody
- Anti-ro antibody
- Anti-smith antibody
- Antibiotic resistance
- Antibiotic-associated colitis
- Antibiotic-associated diarrhea
- Antibiotic
- Antibody
- Anticardiolipin antibody
- Antifungal
- Antimicrobial - induced nephropathy
- Antinuclear antibody
- Antiparasitic
- Antiphospholipid antibody syndrome
- Antiphospholipid antibody
- Antithrombin iii deficiency
- Antiviral
- Anuria
- Anxiety disorder
- Anxiety
- Aortic aneurysm
- Aortic dissection
- Aortic valve atresia
- Aortic valve stenosis
- Aortopulmonary window
- Apathy
- Apgar score at 1 minute
- Apgar score at 10 minutes
- Apgar score at 15 minutes
- Apgar score at 20 minutes
- Apgar score at 5 minutes
- Apgar score
- Apgar test
- Aphagia
- Aphasia
- Apheresis
- Aphonia
- Aphthous ulcer
- Aplasia cutis congenita
- Aplastic anemia due to hepatitis
- Aplastic anemia due to infection
- Aplastic anemia due to radiation
- Aplastic anemia
- Apnea of prematurity
- Apnea
- Apophysitis
- Apparent life threatening event
- Appendicitis
- Appropriate placental villous maturation
- Aprosencephaly
- Arachnoid cyst
- Arachnoiditis
- Arakawa syndrome ii
- Argininosuccinic aciduria
- Aristolochic acid nephropathy
- Arm recoil test
- Arnold-chiari malformation
- Arrest of descent
- Arrest of labor in active phase
- Arrest of labor in second stage
- Arrhythmia
- Arterial catheter
- Arterial embolism
- Arterial ischemic stroke
- Arterial thrombosis related to vascular access complication
- Arterial thrombosis
- Arteriovenous hemangioma
- Arteritis
- Arthralgia
- Arthritis
- Arthrogryposis
- Arthropathy
- Arthropod vector
- Artificial rupture of membranes
- Ascariasis
- Ascending testicle
- Ascites
- Aseptic meningitis
- Asperger syndrome
- Aspergillosis
- Asphyxia
- Aspiration pneumonitis
- Aspiration
- Assisted breech delivery
- Assisted labor
- Asthma
- Astrocytoma
- Ataxia
- Ataxic cerebral palsy
- Atelectasis
- Athetoid cerebral palsy
- Athetosis
- Atrial fibrillation
- Atrial flutter
- Atrial septal defect
- Atrial thrombus
- Atrioventricular block, first degree
- Atrioventricular block, second degree
- Atrioventricular block, third degree
- Attachment parenting
- Attachment theory
- Attending health care provider
- Attention deficit/hyperactivity disorder
- Attenuated bacteria vaccine
- Attenuated live vaccine
- Attenuated live virus vaccine
- Atypical genitalia
- Atypical hemolytic uremic syndrome
- Atypical pneumonia
- Audiometric test
- Auditory hallucination
- Auditory neuropathy spectrum disorder
- Augmentation of labor
- Autism spectrum disorder
- Autism
- Autoimmune adrenalitis
- Autoimmune cytopenia
- Autoimmune disease
- Autoimmune encephalitis
- Autoimmune hemolytic anemia
- Autoimmune hypophysitis
- Autoimmune polyglandular syndrome type 1
- Autoimmune polyglandular syndrome type 2
- Autoimmune polyglandular syndrome(s)
- Autoinflammatory syndrome
- Autologous
- Autonomous ovarian follicular cyst
- Autosomal dominant hypoparathyroidism
- Autosomal dominant hypophosphatemic rickets
- Autosomal dominant neurohypophyseal diabetes insipidus
- Autosomal dominant osteopetrosis
- Autosomal dominant polycystic kidney disease type 2
- Autosomal dominant polycystic kidney disease type I
- Autosomal dominant polycystic kidney disease
- Autosomal recessive hypoparathyroidism
- Autosomal recessive hypophosphatemic rickets
- Autosomal recessive infantile hypercalcemia
- Autosomal recessive osteopetrosis
- Autosomal recessive polycystic kidney disease
- Av fistula aneurysm
- Av fistula maturation failure
- Av fistula stenosis
- Av fistula thrombosis
- Av graft aneurysm
- Av graft stenosis
- Av graft thrombosis
- Avascular necrosis
- Avascular placental villi
- B acute lymphoblastic leukemia
- Babbling
- Babesiosis
- Baby colic
- Baby food
- Baby jumper
- Baby powder
- Baby shampoo
- Baby shower
- Baby talk
- Baby transport
- Baby walker
- Baby-led weaning
- Babysitting
- Babywearing
- Bacillary angiomatosis
- Bacillary peliosis
- Bacillus calmette-guérin vaccine
- Back arching
- Back pain
- Bacteremia
- Bacteria
- Bacterial arthritis
- Bacterial conjunctivitis
- Bacterial endocarditis
- Bacterial gastroenteritis
- Bacterial meningitis
- Bacterial myocarditis
- Bacterial pericarditis
- Bacterial peritonitis
- Bacterial vaginosis
- Balantidiasis
- Band keratopathy
- Barakat syndrome
- Bardet-biedl syndrome
- Barlow's maneuver
- Barth syndrome
- Bartonellosis
- Bartter syndrome
- Basal decidual karyorrhexis
- Basal decidual necrosis
- Basal myofibers
- Baseline fetal heart rate
- Basilar rales
- Basilar-type migraine
- Basophilia
- Basophilopenia
- Bassinet
- Bath ankylosing spondylitis disease activity index
- Bayley scale of infant development I
- Bayley scale of infant development ii
- Bayley scale of infant development iii
- Baylisascariasis
- Beau's lines
- Beckwith-wiedemann syndrome
- Bedwetting
- Behavior during childhood
- Behavior
- Behavioral assessment
- Behavioral development
- Behavioral disorder
- Behavioral insomnia of childhood
- Behavioral rating scale
- Behcet syndrome
- Benign brain tumor
- Benign congenital hypotonia
- Benign familial convulsions
- Benign rolandic epilepsy
- Bernard-soulier syndrome
- Beta thalassemia plus structural variants
- Beta thalassemia
- Beta-ketothiolase deficiency
- Bilateral anophthalmos
- Bilateral cataracts
- Bilateral microphthalmos
- Bilateral optic nerve hypoplasia
- Bilateral renal agenesis
- Bilateral renal dysplasia
- Biliary atresia
- Biliary duct stent
- Bilobate placenta
- Binge eating
- Binocular diplopia
- Bio-inactive somatotropin
- Biologic disease-modifying antirheumatic drug
- Biologic
- Biotinidase deficiency
- Bipolar disorder
- Birmingham vasculitis activity score
- Birth complication
- Birth date
- Birth facility
- Birth head circumference
- Birth injury
- Birth time
- Birth weight
- Bisphosphoglycerate mutase deficiency
- Bisphosphonate - induced nephropathy
- Bladder disorder
- Bladder exstrophy
- Bladder fistula
- Bladder outlet obstruction
- Bladder perforation
- Bladder sphincter dysfunction
- Blanching
- Blast cells present
- Blast crisis
- Blastomycosis
- Blau syndrome
- Bleeding disorder
- Blepharitis
- Blepharospasm
- Blindness
- Blister
- Blomstrand type chondrodysplasia
- Blood glucose measurement
- Blood in stool
- Blood pressure
- Blood product
- Blood transfusion
- Blood urea nitrogen increased
- Bloody discharge
- Blount's disease
- Blunted affect
- Blurred vision
- Body fluid or substance
- Body part
- Body substance discharge
- Body weight
- Bone cancer
- Bone marrow and extramedullary involvement
- Bone marrow involvement
- Bone marrow neoplasm
- Bone marrow transplantation
- Bordetella pertussis
- Bottle feeding
- Botulism
- Bowel obstruction
- Brachial plexopathy
- Brachial plexus injury
- Brachial plexus palsy related to birth
- Bradycardia
- Bradykinesia
- Bradyphagia
- Brain death
- Brain development abnormality
- Brain disorder
- Brain tumor
- Brain-derived neurotropic factor deficiency
- Branch pulmonary artery stenosis
- Branchio-oto-renal syndrome
- Braxton-hicks contraction
- Brazelton neonatal behavorial assessment scale
- Breast cancer
- Breast engorgement in newborn
- Breast feeding
- Breast milk
- Breast pain
- Breast pump
- Breastfeeding and medications
- Breastfeeding and mental health
- Breastfeeding jaundice
- Breastfeeding
- Breastmilk jaundice
- Breath holding
- Breathing effort score
- Breech extraction
- Breech presentation
- British isles lupus assessment group index
- Bronchiolitis
- Bronchitis
- Bronchomalacia
- Bronchopulmonary dysplasia
- Bronchopulmonary sequestration
- Bronchospasm
- Brow presentation
- Brucellosis
- Bruise
- Bruxism
- Bulimia nervosa
- Bulla
- Bullous systemic lupus erythematosus
- Burn
- Burning mouth syndrome
- Butyryl-coa dehydrogenase deficiency
- C-reactive protein
- C1q deficiency
- C1r/c1s deficiency
- C2 deficiency
- C3 deficiency
- C3 glomerulonephritis
- C4 deficiency
- Cacosmia
- Cafe au lait spot
- Calcineurin inhibitor - induced nephropathy
- Calcineurin nephrotoxicity
- Calciphylaxis
- Calcium channel blocker
- Calcium deficiency rickets
- Calcium oxalate urolithiasis
- Calcium phosphate urolithiasis
- Calyceal diverticulum
- Campomelic dysplasia
- Canavan disease
- Cancer
- Candida diaper dermatitis
- Candidiasis
- Caput succedaneum
- Carbamoyl phosphate synthetase deficiency
- Carbohydrate-deficient glycoprotein syndrome
- Cardiac arrest
- Cardiac compression during initial resuscitation
- Cardiac conduction disorder
- Cardiac monitoring
- Cardiac neoplasm
- Cardiac perforation
- Cardiac resuscitation
- Cardiac tamponade
- Cardiofaciocutaneous syndrome
- Cardiomyopathy
- Cardiopulmonary arrest
- Cardiorenal syndrome
- Cardiovascular disorder
- Cardiovascular system finding
- Carney complex
- Carnitine palmitoyltransferase I deficiency
- Carotenoderma
- Carrión disease
- Cat bite
- Cat-scratch disease
- Cataract
- Category I tracing
- Category ii tracing
- Category iii tracing
- Catheter-related inflammation
- Cause of death
- Cecoureterocele
- Cellular congenital mesoblastic nephroma
- Cellular telephone number
- Cellulitis
- Centimeter
- Central adrenal insufficiency
- Central apnea
- Central auditory processing disorder
- Central diabetes insipidus
- Central hearing loss
- Central hyperthyroidism
- Central hypothyroidism
- Central line complication
- Central line infection
- Central nervous system cyst
- Central nervous system disorder
- Central nervous system infectious disease
- Central nervous system involvement
- Central nervous system lupus
- Central nervous system signs and symptoms
- Central obesity
- Central retinal artery occlusion
- Central retinal venous occlusion
- Central sleep apnea
- Central venous access catheter
- Central visual field defect
- Cephalohematoma
- Cercarial dermatitis
- Cerebellar mutism
- Cerebral arterial aneurysm
- Cerebral arteriovenous malformation
- Cerebral atrophy
- Cerebral edema
- Cerebral hemorrhage related to birth
- Cerebral hemorrhage
- Cerebral malaria
- Cerebral palsy
- Cerebral venous aneurysm
- Cerebral visual impairment
- Cerebrospinal fluid leakage
- Cerebrovascular accident
- Cerebrovascular disease
- Cervical carcinoma
- Cervical insufficiency
- Cervical intraepithelial neoplasia
- Cervical meningocele
- Cervical myelocele
- Cervical myelomeningocele
- Cervicitis
- Cesarean birth
- Cesarean hysterectomy
- Chagas disease
- Chalazion
- Characteristic
- Charge syndrome
- Chediak-higashi syndrome
- Cheilitis
- Cheiromegaly
- Chemical burn of eye
- Chemical conjunctivitis
- Chemical peritonitis
- Chemotherapeutic drug - induced nephropathy
- Chest pain
- Chest tube
- Chikungunya
- Child abuse
- Child custody
- Child health questionnaire
- Child neglect
- Child
- Childbirth
- Childhood acute erythroid leukemia
- Childhood acute lymphoblastic leukemia
- Childhood acute megakaryoblastic leukemia
- Childhood acute monoblastic and monocytic leukemia
- Childhood acute monoblastic leukemia
- Childhood acute monocytic leukemia
- Childhood acute myeloid leukemia with abnormalities of chromosome 5q
- Childhood acute myeloid leukemia with abnormalities of chromosome 7
- Childhood acute myeloid leukemia with maturation
- Childhood acute myeloid leukemia with minimal differentiation
- Childhood acute myeloid leukemia with nup98 rearrangement
- Childhood acute myeloid leukemia without maturation
- Childhood acute myeloid leukemia, not otherwise specified
- Childhood acute myeloid leukemia
- Childhood acute myelomonocytic leukemia
- Childhood alveolar rhabdomyosarcoma
- Childhood alveolar soft part sarcoma
- Childhood anaplastic astrocytoma
- Childhood anaplastic ependymoma
- Childhood anaplastic large cell lymphoma
- Childhood anaplastic oligoastrocytoma
- Childhood anaplastic oligodendroglioma
- Childhood angiosarcoma
- Childhood astrocytic tumor
- Childhood astrocytoma
- Childhood atypical choroid plexus papilloma
- Childhood atypical teratoid/rhabdoid tumor
- Childhood b acute lymphoblastic leukemia
- Childhood b lymphoblastic lymphoma
- Childhood botryoid-type embryonal rhabdomyosarcoma
- Childhood brain neoplasm
- Childhood brain stem astrocytoma
- Childhood brain stem glioma
- Childhood brain stem gliosarcoma
- Childhood brain stem mixed glioma
- Childhood brain stem tumor
- Childhood breast carcinoma
- Childhood burkitt leukemia
- Childhood burkitt lymphoma
- Childhood carcinoid tumor
- Childhood central nervous system choriocarcinoma
- Childhood central nervous system embryonal carcinoma
- Childhood central nervous system embryonal neoplasm
- Childhood central nervous system germ cell tumor
- Childhood central nervous system germinoma
- Childhood central nervous system immature teratoma
- Childhood central nervous system mature teratoma
- Childhood central nervous system mixed germ cell tumor
- Childhood central nervous system neoplasm
- Childhood central nervous system primitive neuroectodermal tumor
- Childhood central nervous system teratoma
- Childhood central nervous system yolk sac tumor
- Childhood cerebellar tumor
- Childhood cerebral ganglioneuroblastoma
- Childhood cerebral neuroblastoma
- Childhood choriocarcinoma
- Childhood choroid plexus carcinoma
- Childhood choroid plexus neoplasm
- Childhood chronic myelogenous leukemia, bcr-abl1 positive
- Childhood classical hodgkin lymphoma
- Childhood clear cell sarcoma of soft tissue
- Childhood colorectal carcinoma
- Childhood conventional osteosarcoma
- Childhood craniopharyngioma
- Childhood depression
- Childhood desmoplastic small round cell tumor
- Childhood diffuse astrocytoma
- Childhood diffuse large b-cell lymphoma
- Childhood disintegrative disorder
- Childhood dysgerminoma
- Childhood embryonal carcinoma
- Childhood embryonal rhabdomyosarcoma
- Childhood ependymal tumor
- Childhood ependymoblastoma
- Childhood ependymoma
- Childhood epithelioid sarcoma
- Childhood esophageal carcinoma
- Childhood extracranial germ cell tumor
- Childhood extragonadal malignant germ cell tumor
- Childhood extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue
- Childhood extraskeletal osteosarcoma
- Childhood fibrillary astrocytoma
- Childhood fibrosarcoma
- Childhood follicular lymphoma
- Childhood ganglioglioma
- Childhood ganglioneuroblastoma
- Childhood gastric carcinoma
- Childhood gastrointestinal stromal tumor
- Childhood gemistocytic astrocytoma
- Childhood germ cell tumor
- Childhood germinomatous germ cell tumor
- Childhood giant cell glioblastoma
- Childhood glioblastoma
- Childhood gliomatosis cerebri
- Childhood gliosarcoma
- Childhood gonadal germ cell tumor
- Childhood health assessment questionnaire
- Childhood hepatocellular carcinoma
- Childhood hodgkin lymphoma
- Childhood immature teratoma
- Childhood immunizations in the United States
- Childhood immunoblastic lymphoma
- Childhood intermixed ganglioneuroblastoma
- Childhood intracranial neoplasm
- Childhood langerhans cell histiocytosis with risk organ involvement
- Childhood langerhans cell histiocytosis
- Childhood laryngeal carcinoma
- Childhood leiomyosarcoma
- Childhood leptomeningeal melanoma
- Childhood leukemia
- Childhood linear iga disease
- Childhood liposarcoma
- Childhood lymphoblastic lymphoma
- Childhood lymphocyte-depleted classical hodgkin lymphoma
- Childhood lymphocyte-rich classical hodgkin lymphoma
- Childhood lymphoma
- Childhood lymphomatoid granulomatosis
- Childhood malignant kidney tumor
- Childhood malignant liver tumor
- Childhood malignant ovarian germ cell tumor
- Childhood malignant peripheral nerve sheath tumor
- Childhood malignant testicular germ cell tumor
- Childhood mature t- and nk-cell lymphoma
- Childhood mature teratoma
- Childhood medulloblastoma
- Childhood melanoma
- Childhood meningioma
- Childhood mesenchymal chondrosarcoma
- Childhood mixed cellularity classical hodgkin lymphoma
- Childhood mixed germ cell tumor
- Childhood mixed glioma
- Childhood myelodysplastic syndrome
- Childhood myositis assessment scale
- Childhood myxoid chondrosarcoma
- Childhood myxopapillary ependymoma
- Childhood nasal cavity carcinoma
- Childhood nasal type extranodal nk/t-cell lymphoma
- Childhood neuroblastoma
- Childhood nodal marginal zone lymphoma
- Childhood nodular ganglioneuroblastoma
- Childhood nodular lymphocyte predominant hodgkin lymphoma
- Childhood nodular sclerosis classical hodgkin lymphoma
- Childhood non-germinomatous germ cell tumor
- Childhood non-hodgkin lymphoma
- Childhood obesity
- Childhood oligoastrocytoma
- Childhood oligodendroglioma
- Childhood osteosarcoma
- Childhood ovarian choriocarcinoma
- Childhood ovarian embryonal carcinoma
- Childhood ovarian germ cell tumor
- Childhood ovarian immature teratoma
- Childhood ovarian mature teratoma
- Childhood ovarian mixed germ cell tumor
- Childhood ovarian non-germinomatous germ cell tumor
- Childhood ovarian teratoma
- Childhood ovarian yolk sac tumor
- Childhood overweight
- Childhood paranasal sinus carcinoma
- Childhood parathyroid gland carcinoma
- Childhood parosteal osteosarcoma
- Childhood periosteal osteosarcoma
- Childhood pilocytic astrocytoma
- Childhood pilomyxoid astrocytoma
- Childhood pineal parenchymal cell neoplasm
- Childhood pineal parenchymal tumor of intermediate differentiation
- Childhood pineoblastoma
- Childhood pleomorphic rhabdomyosarcoma
- Childhood pleomorphic xanthoastrocytoma
- Childhood primary cutaneous anaplastic large cell lymphoma
- Childhood protoplasmic astrocytoma
- Childhood renal cell carcinoma
- Childhood rhabdomyosarcoma
- Childhood salivary gland carcinoma
- Childhood schizophrenia
- Childhood seminoma
- Childhood small intestinal carcinoma
- Childhood small intestine leiomyosarcoma
- Childhood soft tissue sarcoma
- Childhood spinal cord tumor
- Childhood spindle cell rhabdomyosarcoma
- Childhood supratentorial primitive neuroectodermal tumor
- Childhood synovial sarcoma
- Childhood systemic anaplastic large cell lymphoma
- Childhood t acute lymphoblastic leukemia
- Childhood t lymphoblastic lymphoma
- Childhood teratoma
- Childhood testicular choriocarcinoma
- Childhood testicular embryonal carcinoma
- Childhood testicular germ cell tumor
- Childhood testicular immature teratoma
- Childhood testicular mature teratoma
- Childhood testicular mixed embryonal carcinoma and teratoma
- Childhood testicular mixed germ cell tumor
- Childhood testicular non-seminomatous germ cell tumor
- Childhood testicular teratoma
- Childhood testicular yolk sac tumor
- Childhood thyroid gland carcinoma
- Childhood thyroid gland follicular carcinoma
- Childhood thyroid gland medullary carcinoma
- Childhood thyroid gland papillary carcinoma
- Childhood visual pathway astrocytoma
- Childhood visual pathway glioma
- Childhood wilms tumor
- Childhood yolk sac tumor
- Childhood-onset systemic lupus erythematosus
- Childhood
- Chills
- Chlamydial conjunctivitis
- Chloroquine compound
- Choking
- Cholangitis
- Cholecystitis
- Choledochal cyst
- Cholelithiasis
- Cholestasis
- Cholesterol side-chain cleavage deficiency
- Chondrodysplasia punctata
- Chondroectodermal dysplasia
- Chorangioma
- Chorangiosis
- Chorea
- Choreoathetosis
- Chorioamnionitis
- Chorionic plate vessel thrombus
- Chorionic villus sampling
- Chorioretinitis
- Choroid plexus cyst
- Chromosomal abnormality
- Chromosome 16p11.2 deletion syndrome
- Chromosome 18q deletion syndrome
- Chronic choriodeciduitis
- Chronic decubitus
- Chronic graft versus host disease
- Chronic kidney allograft nephropathy
- Chronic kidney disease
- Chronic liver disease
- Chronic lung disease
- Chronic maternal hypertension with superimposed preeclampsia
- Chronic maternal hypertension
- Chronic migraine
- Chronic pain
- Chronic plasma cell deciduitis
- Chronic pyelonephritis
- Chronic recurrent multifocal osteomyelitis
- Chronic renal failure
- Chronic sinusitis
- Chronic suppurative otitis media
- Chronic tic disorder
- Chronic urate nephropathy
- Chronic uteroplacental vasculitis
- Chronic uveitis
- Chronic villitis
- Chronological age
- Chylothorax
- Ciliary motility defect
- Circumcision
- Circummarginate placenta
- Circumscribed morphea
- Circumvallate placenta
- Cirrhosis
- Citrullinemia
- City
- Classic congenital adrenal hyperplasia
- Classic congenital mesoblastic nephroma
- Classic creutzfeldt-jakob disease
- Classical phenylketonuria
- Clear cell sarcoma of the kidney
- Cleft lip
- Cleft palate
- Cleidocranial dysostosis
- Clinical assessment tool
- Clinical chorioamnionitis
- Clonus
- Closed adoption
- Closed angle glaucoma
- Closed fracture
- Closed globe injury
- Clostridium difficile infection
- Closure patent ductus arteriosus
- Cloth diaper
- Clubbing of fingers
- Cluster headache
- Coagulation disorder related to liver dysfunction
- Coagulation disorder
- Coagulation factor deficiency
- Coarctation of aorta
- Coccidioidomycosis
- Coccygeal sinus
- Cogan-reese syndrome
- Cognitive assessment
- Cognitive development
- Cognitive impairment
- Cole-carpenter syndrome
- Colic
- Colitis
- Collapsed lung
- Collapsing glomerulopathy
- Collection date
- Collection time
- Coloboma of eyelid
- Coloboma of iris
- Coloboma of retina
- Colon atresia
- Colonic band
- Colonic fistula
- Colonic stenosis
- Colonic web
- Colonization
- Color blindness
- Colostomy site
- Coma
- Common atrioventricular canal
- Common ventricle
- Communicating hydrocephalus
- Community-acquired pneumonia
- Compartment syndrome
- Compensated hypothyroidism
- Complement c3
- Complement c4
- Complement deficiency
- Complement hemolytic activity assay
- Complete abortion
- Complete atrioventricular canal defect (balanced)
- Complete atrioventricular canal defect (unbalanced)
- Complete hydatidiform mole
- Complete maternal surface of placenta
- Complete resection
- Complete trisomy 13 syndrome
- Complete trisomy 21 syndrome
- Complex cyst of kidney
- Complex regional pain syndrome I
- Complex regional pain syndrome ii
- Complex tic
- Complication
- Compound fetal presentation
- Compulsive behavior
- Conception age
- Concussion
- Conduct disorder
- Conductive hearing loss
- Condyloma acuminatum
- Confusion
- Confusional arousal
- Congenital adrenal hyperplasia
- Congenital amegakaryocytosis
- Congenital anemia
- Congenital anomaly of pulmonary veins
- Congenital aortic arch hypoplasia
- Congenital bilateral cataracts
- Congenital bleeding disorder
- Congenital bundle of his tachycardia
- Congenital cardiovascular abnormality
- Congenital cataract
- Congenital central hypoventilation
- Congenital cerebellar hypoplasia
- Congenital chylothorax
- Congenital complete atrioventricular block
- Congenital cystic adenomatoid malformation of lung
- Congenital cystic hygroma
- Congenital cytomegaloviral infection
- Congenital deformation
- Congenital diaphragmatic hernia
- Congenital disorder
- Congenital disruption
- Congenital dyserythropoietic anemia
- Congenital dysplasia
- Congenital facial nerve palsy
- Congenital gastrointestinal disorder
- Congenital generalized lipodystrophy
- Congenital genitourinary abnormality
- Congenital growth hormone deficiency
- Congenital h-type tracheoesophageal fistula
- Congenital hamartoma
- Congenital heart disease
- Congenital hematological disorder
- Congenital hydrocephalus
- Congenital hydronephrosis
- Congenital hydroureter
- Congenital hypergonadotropic hypogonadism
- Congenital hyperinsulinism
- Congenital hyperthyroidism
- Congenital hypogonadotropic hypogonadism
- Congenital hypothyroidism
- Congenital ileal stenosis
- Congenital isolated adrenocorticotropic hormone deficiency
- Congenital isolated thyroid stimulating hormone deficiency
- Congenital jejunal stenosis
- Congenital lipoid adrenal hyperplasia
- Congenital listeriosis
- Congenital lobar emphysema
- Congenital lung malformation
- Congenital malformation syndrome related to known exogenous cause
- Congenital malformation syndrome
- Congenital malformation
- Congenital melanocytic nevus
- Congenital mesoblastic nephroma
- Congenital metabolic disorder
- Congenital methemoglobinemia
- Congenital musculoskeletal defect
- Congenital myotonic dystrophy
- Congenital nephrotic syndrome - cytomegalovirus associated
- Congenital nephrotic syndrome - diffuse mesangial sclerosis
- Congenital nephrotic syndrome - focal segmental glomerulosclerosis
- Congenital nephrotic syndrome - infection associated
- Congenital nephrotic syndrome - rubivirus associated
- Congenital nephrotic syndrome - toxoplasma associated
- Congenital nephrotic syndrome - treponema pallidum associated
- Congenital nephrotic syndrome
- Congenital nervous system disorder
- Congenital neurogenic bladder
- Congenital or acquired anatomic abnormality
- Congenital ovarian failure
- Congenital partial lipodystrophy
- Congenital phrenic nerve injury
- Congenital phrenic nerve palsy
- Congenital postural scoliosis
- Congenital pulmonary lymphangiectasia
- Congenital pulmonary valve insufficiency
- Congenital pure red cell aplasia
- Congenital renal hypoplasia
- Congenital reproductive system abnormality
- Congenital respiratory system disorder
- Congenital rubella syndrome
- Congenital septal defect
- Congenital skin disorder
- Congenital supraventricular tachycardia
- Congenital syphilis
- Congenital systemic disorder
- Congenital testicular failure
- Congenital thrombotic thrombocytopenic purpura
- Congenital unilateral cataract
- Congenital ureteropelvic junction obstruction
- Congenital ureterovesical junction obstruction
- Congenital urinary system abnormality
- Congenital urinary tract obstruction
- Congenital varicella syndrome
- Congenital varicella zoster infection
- Congenital vena cava abnormality
- Congenital ventricular tachycardia
- Congential aortic valve insufficiency
- Congestive heart failure
- Congruent visual field defect
- Conjoined twins
- Conjugate vaccine
- Conjugated hyperbilirubinemia
- Conjunctival foreign body
- Conjunctivitis
- Conn syndrome
- Connective tissue disorder
- Connective tissue
- Constipation
- Consumptive coagulopathy
- Contact dermatitis
- Contact transmission
- Continent epispadias
- Contrasexual sexual development
- Contrast - induced nephropathy
- Contrast agent
- Contusion
- Coombs test positive
- Coprolalia
- Cor pulmonale
- Cor triatriatum
- Cord blood transplantation
- Corneal abrasion
- Corneal dellen
- Corneal foreign body
- Cornelia de lange syndrome
- Cornual pregnancy
- Coronary anomaly
- Coronary artery stent
- Corpus callosum agenesis
- Corrected age
- Cortical blindness
- Corticosteroid
- Corticotropin-releasing hormone deficiency
- Costello syndrome
- Cough
- Cradle cap
- Cranial nerve disorder
- Cranial suture separation
- Craniodiaphyseal dysplasia
- Craniofacial dysostosis
- Craniopharyngioma
- Craniorachischisis
- Craniosynostosis
- Craniotabes
- Craniotubular hyperostosis
- Crawling (human)
- Crescentic glomerulonephritis
- Cri du chat syndrome
- Crimean-congo hemorrhagic fever
- Crohn's disease
- Cross eyed
- Croup
- Crown to rump length measurement
- Cry room
- Crying#Types of crying in infants
- Crying
- Cryoglobulinemic glomerulonephritis secondary to systemic disease
- Cryoglobulinemic glomerulonephritis
- Cryopyrin-associated periodic syndrome
- Cryptococcosis
- Cryptophthalmos syndrome
- Cryptorchidism
- Cryptosporidiosis
- Crystalline lens dislocation
- Cuffed hemodialysis catheter
- Cuffed peritoneal dialysis catheter
- Cushing disease
- Cushing syndrome
- Cushingoid
- Cutaneous assessment tool
- Cutaneous dermatomyositis disease area and severity index
- Cutaneous fistula
- Cutaneous lupus erythematosus
- Cutaneous polyarteritis nodosa
- Cutaneous vasculitis
- Cutting behavior
- Cyanosis
- Cyanotic body
- Cyanotic limbs
- Cyclic citrullinated peptide antibody
- Cyclic neutropenia
- Cyclical vomiting
- Cyclosporiasis
- Cyst
- Cystic fibrosis pulmonary exacerbation
- Cystic fibrosis with meconium ileus
- Cystic fibrosis
- Cystic hygroma
- Cystic kidney disease
- Cystic partially differentiated nephroblastoma
- Cystic periventricular leukomalacia
- Cysticercosis
- Cystine urolithiasis
- Cystitis
- Cystoid macular edema
- Cystoisosporiasis
- Cystostomy site
- Cytochrome-c oxidase deficiency
- Cytokine release syndrome
- Dandy-walker syndrome
- Date
- Dax1 deficiency
- Daycare
- Deafness
- Death
- Deceased sibling
- Deciduitis
- Decreased attention
- Decreased best corrected visual acuity
- Decreased bladder compliance
- Decreased bone density
- Decreased concentration
- Decreased libido
- Decreased physical activity
- Decreased uncorrected visual acuity
- Decreased visual acuity with current correction
- Decreased visual acuity
- Decubitus
- Deep circumscribed morphea
- Deep venous thrombosis
- Defective thyroglobulin synthesis
- Defective thyroglobulin transport
- Deficiency of the interleukin-1 receptor antagonist
- Deficiency of the interleukin-36 receptor antagonist
- Dehydration
- Deiodinase deficiency
- Delayed epiphyseal fusion
- Delayed graft function
- Delayed puberty
- Delirium
- Delivery by destructive operation
- Delivery procedure
- Delusion
- Demographics
- Demyelinating disorder
- Dengue
- Dense deposit disease
- Dental caries
- Dental disorder
- Dental fluorosis
- Denver development screening test
- Denys-drash syndrome, incomplete
- Denys-drash syndrome
- Depigmentation
- Depressed level of consciousness
- Depressed mood
- Dermatographism
- Dermatomyositis skin severity index
- Dermatophytosis
- Dermoid cyst
- Desmoplastic infantile astrocytoma
- Desmoplastic infantile ganglioglioma
- Desquamation
- Developmental delay
- Developmental disorder
- Developmental dysplasia of hip
- Developmental dyspraxia
- Developmental milestone
- Device complication
- Device embolization
- Device migration
- Device
- Dextro-transposition of the great arteries
- Dextrocardia situs solitus
- Dextrocardia
- Diabetes insipidus
- Diabetes mellitus
- Diabetic embryopathy
- Diabetic fetopathy
- Diabetic ketoacidosis
- Diabetic nephropathy
- Diabetic retinopathy
- Diagnosis
- Diagnostic procedure
- Dialysis access complication
- Dialysis catheter embolism
- Dialysis catheter exit site infection
- Dialysis catheter fracture
- Dialysis catheter infection
- Dialysis catheter obstruction
- Dialysis catheter tunnel infection
- Dialysis membrane reaction
- Dialyzer blood leak
- Diaper bag
- Diaper dermatitis
- Diaper rash
- Diaper
- Diaphoresis
- Diaphragmatic eventration
- Diaphragmatic hernia
- Diarrhea-associated hemolytic uremic syndrome
- Diarrhea
- Diastematomyelia
- Dichorionic diamniotic twin pregnancy
- Diencephalic syndrome of infancy
- Diethylstilbestrol syndrome
- Differences of sex development
- Diffuse cutaneous systemic sclerosis
- Diffuse endocapillary glomerulonephritis
- Diffuse goiter
- Diffuse katp-associated hyperinsulinism
- Digital fetal scalp stimulation
- Dilated cardiomyopathy
- Dimorphic fungus
- Diphtheria toxoid/tetanus toxoid vaccine adsorbed
- Diphtheria toxoid/tetanus toxoid/acellular pertussis vaccine
- Diphtheria toxoid/tetanus toxoid/inactivated pertussis vaccine dtp
- Diphtheria
- Diphyllobothriasis
- Diplegia
- Diplopia
- Dipsogenic diabetes insipidus
- Direct inguinal hernia
- Direct maternal death
- Direct transmission
- Disclaimer
- Discoid lupus erythematosus
- Discoid rash
- Discordant twin
- Discordant ventriculoarterial connection
- Disease Index
- Disease or disorder
- Disease-modifying antirheumatic drug
- Disinhibited
- Dislodged catheter
- Dislodged peritoneal dialysis catheter
- Disorder of androgen synthesis
- Disordered eating
- Disordered thinking
- Displaced peritoneal dialysis catheter
- Disrupted suture
- Disseminated bacillus calmette-guérin infection
- Disseminated candidiasis
- Disseminated intravascular coagulation
- Disseminated juvenile xanthogranuloma
- Disseminated listeriosis
- Disseminated varicella zoster vaccine virus infection
- Distal 18q deletion syndrome
- Distal renal tubular acidosis
- Disturbance of temperature regulation
- Dizziness
- Doctor's information
- Dog bite
- Donohue syndrome
- Double cortex syndrome
- Double outlet right ventricle
- Dracunculiasis
- Dravet syndrome
- Drooling
- Droplet transmission
- Drug exposure via breast milk
- Drug induced cutaneous lupus erythematosus
- Drug induced cutaneous vasculitis
- Drug induced lupus erythematosus
- Drug rash
- Drug reaction with eosinophilia and systemic symptoms
- Drug therapy
- Drug use history
- Drug withdrawal
- Drug-induced aplastic anemia
- Drug-induced kidney injury
- Drug-induced methemoglobinemia
- Drug-induced thrombocytopenia
- Drug-induced tubulointerstitial nephritis
- Drug/toxin-induced aplastic anemia
- Drugs
- Dry eye
- Dual oxidase 2 deficiency
- Dubowitz score
- Ductus venosus agenesis
- Duodenal atresia
- Duodenal band
- Duodenal stenosis
- Duodenal web
- Duodenostomy site
- Duplex kidney
- Duplicated ureter
- Duration of rupture of membranes
- Dwarfism
- Dyscalculia
- Dysequilibrium syndrome
- Dysesthesia
- Dysfibrinogenemia
- Dysfunctional elimination syndrome
- Dysfunctional labor
- Dysgerminoma
- Dysgeusia
- Dyskinesia
- Dyslexia
- Dysmenorrhea
- Dysmyelination
- Dysosmia
- Dyspepsia
- Dysphagia
- Dysphasia
- Dysphonia
- Dyspnea
- Dystonia
- Dysuria
- Ear dimple
- Ear tag
- Early adolescence
- Early childhood
- Early disseminated lyme disease
- Early fetal death
- Early fetal heart rate deceleration
- Early infantile epileptic encephalopathy with burst-suppression
- Early inflammatory arthritis
- Early latent syphilis
- Early localized lyme disease
- Early myoclonic encephalopathy
- Early neonatal mortality
- Early onset primary dystonia
- Early postpartum hemorrhage
- Early pregnancy loss
- Early prosthetic valve endocarditis
- Early relapse of acute lymphoblastic leukemia
- Early relapse
- Early rheumatoid arthritis
- Early term birth
- Easy bruising
- Eating disorder
- Ebola
- Ebstein anomaly
- Ecchymosis
- Echinococcosis
- Echolalia
- Eclampsia
- Ectodermal dysplasia
- Ectopic acth syndrome
- Ectopic atrial tachycardia
- Ectopic posterior pituitary
- Ectopic pregnancy
- Ectopic thyroid gland
- Ectopic ureter
- Ectopic ureterocele
- Ectrodactyly
- Eczema
- Edema
- Education level
- Effusion
- Ehlers-danlos syndrome
- Eiken type chondrodysplasia
- Ejaculatory dysfunction
- Elective cesarean delivery
- Electrolyte disorder
- Elevated blood pressure measurement
- Elevated serum alkaline phosphatase
- Elevated test result
- Elliptocytosis
- Embolism
- Embryonic loss
- Embryonic stage
- Emergency cesarean delivery
- Empty sella syndrome
- Empyema
- Enanthem
- Encephalitis
- Encephalocele
- Encephalomalacia
- Encephalomyelitis
- Encephalopathy of prematurity
- Encephalopathy
- Encopresis
- End-stage liver disease
- Endemic cretinism
- Endemic typhus
- Endocardial fibroelastosis
- Endocarditis
- Endocrine neoplasm
- Endocrine system disorder
- Endocrine system finding
- Endogenous infection
- Endophthalmitis
- Endosteal hyperostosis
- Enlarged abdomen
- Enophthalmos
- Enteral tube feeding
- Enteric hyperoxaluria
- Enteritis
- Enterobiasis
- Enterocolitis
- Enterostomy prolapse
- Enterostomy site
- Enthesitis-related arthritis
- Enthesitis
- Enzyme deficiency
- Eosinophilia
- Eosinophilic fasciitis
- Eosinophilic meningitis
- Eosinophilopenia
- Ependymoma
- Epidemic typhus
- Epidermolysis bullosa aquisita
- Epidermolysis bullosa
- Epidural block
- Epidural hematoma
- Epidural hemorrhage
- Epigastric hernia
- Epiglottitis
- Epilepsy
- Epiphysiolysis
- Episcleritis
- Episodic fetal heart rate pattern
- Epispadias
- Epistaxis
- Epstein syndrome
- Erb's palsy
- Erectile dysfunction
- Erosion
- Erythema infectiosum
- Erythema migrans
- Erythema multiforme
- Erythema toxicum neonatorum
- Erythema
- Erythrocyte adenylate kinase deficiency
- Erythrocyte enolase deficiency
- Erythrocyte sedimentation rate
- Erythrocytosis
- Escobar syndrome
- Esophageal atresia
- Esophageal candidiasis
- Esophageal duplication
- Esophageal dysphagia
- Esophageal fistula
- Esophageal perforation
- Esophageal varices
- Esophageal web
- Esophagitis
- Essential thrombocythemia
- Estimated due date
- Ethnic group
- Euphoria
- European league against rheumatism classification criteria for juvenile chronic arthritis
- Euthyroid condition
- Euthyroid goiter
- Evaluation procedure
- Evans syndrome
- Ewing sarcoma
- Exanthem
- Excessive bleeding
- Excessive bruising
- Excessive sucking
- Excessive weight gain in pregnancy
- Excoriation
- Exfoliative dermatitis
- Exogenous obesity
- Exophthalmos
- Exsanguination
- Extended oligoarticular juvenile idiopathic arthritis
- Extensively drug-resistant mycobacterium tuberculosis
- Extensively drug-resistant tuberculosis
- External compression headache
- External fetal heart rate monitoring
- External hydrocephalus
- Extracorporeal circuit clot
- Extragonadal germ cell tumor
- Extramedullary involvement
- Extraocular retinoblastoma
- Extraosseous calcification
- Extrarenal rhabdoid tumor
- Extremely low birth weight
- Extremely preterm infant
- Eye discharge
- Eye disorder
- Eye finding
- Eye prophylaxis
- Eye redness
- Fabry disease
- Face presentation
- Facial nerve palsy related to birth
- Facial nerve palsy related to trauma
- Facial nerve palsy
- Factor I deficiency
- Factor I inactivation
- Factor ii deficiency
- Factor ii inactivation
- Factor iii inactivation
- Factor ix inactivation
- Factor v deficiency
- Factor v inactivation
- Factor v leiden
- Factor vii deficiency
- Factor vii inactivation
- Factor viii inactivation
- Factor x deficiency
- Factor x inactivation
- Factor xi deficiency
- Factor xi inactivation
- Factor xii deficiency
- Factor xii inactivation
- Factor xiii deficiency
- Factor xiii inactivation
- Failure of catch-up growth
- Failure to thrive
- Fall
- Familial atypical hemolytic uremic syndrome
- Familial cold autoinflammatory syndrome
- Familial dysalbuminemic hyperthyroxinemia
- Familial glucocorticoid deficiency type 1
- Familial glucocorticoid deficiency type 2
- Familial glucocorticoid deficiency type 3
- Familial glucocorticoid deficiency type 4
- Familial hemiplegic migraine
- Familial hyperaldosteronism type 1
- Familial hyperaldosteronism type 2
- Familial hyperaldosteronism type 3
- Familial hyperaldosteronism
- Familial hypercalciuric hypocalcemia
- Familial hypocalciuric hypercalcemia
- Familial idiopathic short stature
- Familial idiopathic tall stature
- Familial isolated hyperparathyroidism
- Familial male precocious puberty
- Familial mediterranean fever
- Familial primary hypomagnesemia
- Fanconi anemia
- Fanconi syndrome
- Fasciculation
- Fasciitis
- Fasciolopsiasis
- Fasciolosis
- Fat adherence syndrome
- Fatigue
- Febrile seizure
- Fecal incontinence
- Fecal-oral transmission
- Fechtner syndrome
- Feeding intolerance
- Feeding method
- Feeding tube complication
- Feeding tube
- Female reproductive system disorder
- Female
- Feminization in boys
- Femur fracture
- Fetal acidemia
- Fetal alcohol spectrum disorder
- Fetal alcohol syndrome
- Fetal arrhythmia
- Fetal assessment
- Fetal biophysical profile
- Fetal blood loss
- Fetal bradyarrhythmia
- Fetal bradycardia
- Fetal chorionic vasculitis
- Fetal circulation with increased nucleated erythrocytes
- Fetal death
- Fetal disorder
- Fetal doppler velocimetry
- Fetal echocardiography
- Fetal fibronectin test
- Fetal finding
- Fetal heart deceleration
- Fetal heart finding
- Fetal heart rate acceleration
- Fetal heart rate monitoring
- Fetal heart rate variability
- Fetal heart rate
- Fetal heart rhythm
- Fetal heart tone location
- Fetal heart tone
- Fetal hydantoin syndrome
- Fetal hypoxemia
- Fetal hypoxia
- Fetal large for gestational age
- Fetal macrosomia
- Fetal malpresentation
- Fetal methotrexate syndrome
- Fetal neurodevelopmental disorder
- Fetal pulse oximetry
- Fetal restitution
- Fetal retinoid syndrome
- Fetal scalp sampling
- Fetal small for gestational age with abnormal dopplers
- Fetal small for gestational age with oligohydramnios
- Fetal stage
- Fetal stem vessel thrombus with or without dystrophic calcification
- Fetal stem vessel thrombus
- Fetal tachyarrhythmia
- Fetal tachycardia
- Fetal valproate syndrome
- Fetal virilization
- Fetal warfarin syndrome
- Fetal-maternal hemorrhage
- Fetus small for gestational age
- Fetus
- Fever
- Fibrodysplasia ossificans progressiva
- Fibromyalgia
- Fibrosarcoma
- Fibula fracture
- Filamentous fungus
- Filariasis
- Finding
- Fine motor delay
- Finnegan score measurement
- First degree burn
- First degree perineal laceration
- First feeding
- First relapse
- First trimester antepartum hemorrhage
- Fisher syndrome
- Fissuring
- Fistula discharge
- Fistula
- Five minutes after birth
- Fixed drug eruption
- Flat affect
- Flatulence
- Flight of ideas
- Floaters
- Floppy infant
- Flt3 internal tandem duplication
- Flt3-internal tandem duplication high allelic ratio
- Flu-like symptoms
- Flushing
- Focal and segmental proliferative glomerulonephritis
- Focal katp-associated hyperinsulinism
- Focal lipodystrophy
- Focal segmental glomerulosclerosis cellular variant
- Focal segmental glomerulosclerosis collapsing variant
- Focal segmental glomerulosclerosis perihilar variant
- Focal segmental glomerulosclerosis tip lesion variant
- Focal segmental glomerulosclerosis, not otherwise specified
- Focal segmental glomerulosclerosis
- Focal seizure
- Follicle stimulating hormone deficiency
- Follicle stimulating hormone receptor deficiency
- Follicle stimulating hormone-producing adenoma
- Follicular thyroid carcinoma
- Follicular thyroid tumor
- Folliculitis
- Fontanel depressed
- Fontanelle bulging
- Fontanelle
- Foodborne botulism
- Foodborne illness
- Forceps assisted vaginal delivery
- Forceps injury
- Foreign body ingestion
- Foster care
- Fourth degree perineal laceration
- Fracture of clavicle related to birth
- Fracture of femur related to birth
- Fracture of humerus related to birth
- Fracture of long bone related to birth
- Fracture of nose related to birth
- Fracture of radius related to birth
- Fracture of skull related to birth
- Fracture of spine related to birth
- Fracture of ulna related to birth
- Fracture related to birth
- Fracture
- Fragile x syndrome
- Frank umbilical cord prolapse
- Frasier syndrome
- Freeman-sheldon syndrome
- Frenulum
- Fryns syndrome
- Fucosidosis
- Full term birth
- Full term neonatal stage
- Functional hearing loss
- Functional intestinal obstruction
- Functional pituitary macroadenoma
- Functional pituitary microadenoma
- Fungal infection
- Fungal keratitis
- Fungal pericarditis
- Fungus
- Funic presentation
- Funisitis
- Fused eyelid
- Fused placenta
- Fusion-negative alveolar rhabdomyosarcoma
- Fusion-positive alveolar rhabdomyosarcoma
- Gagging
- Gait unsteady
- Galactorrhea
- Galactose measurement
- Galactose-1-phosphate uridyltransferase measurement
- Galactosemia
- Galeazzi test
- Gamma-delta t-cell depletion
- Gangrenous umbilical hernia
- Gasping syndrome
- Gastritis
- Gastroenteritis
- Gastroesophageal reflux disease
- Gastroesophageal reflux
- Gastrointestinal bleed
- Gastrointestinal disorder
- Gastrointestinal fistula
- Gastrointestinal perforation
- Gastrointestinal system signs and symptoms
- Gastroparesis
- Gastroschisis
- Gastrostomy site
- Gaucher disease
- General anesthesia procedure
- General appearance
- Generalized anxiety disorder
- Generalized lipodystrophy
- Generalized morphea
- Generalized thyroid hormone resistance
- Genetic disorder
- Genetic testing
- Genital herpes
- Genu recurvatum
- Germ cell tumor
- Germinal matrix hemorrhage of newborn
- Germinoma
- Germinomatous germ cell tumor
- Gesell developmental schedule
- Gestational age
- Gestational diabetes mellitus, a1
- Gestational diabetes mellitus, a2
- Gestational diabetes mellitus
- Gestational hypertension
- Gingivitis
- Gitelman syndrome
- Glanders
- Glanzmann thrombasthenia
- Glaucoma
- Glioma
- Globus
- Glomerulocystic disease
- Glomerulomegaly
- Glomerulonephritis
- Glomerulopathy
- Glomerulosclerosis
- Glossaries
- Glossary of medical terms
- Glossitis
- Glucagon deficiency
- Glucocorticoid resistance
- Glucocorticoid suppressible hyperaldosteronism
- Glucocorticoid
- Glucokinase-associated diabetes mellitus
- Glucokinase-associated hyperinsulinism
- Glucose intolerance
- Glucose phosphate isomerase deficiency
- Glucose-6-phosphate dehydrogenase deficiency
- Glutamate dehydrogenase 1 hyperinsulinism
- Glutaric aciduria, type 1
- Glutaric aciduria, type 2
- Glycine encephalopathy
- Glycogen storage disease type vii
- Glycogen storage disease
- Gnathostomiasis
- Goiter
- Goldenhar syndrome
- Gonadal agenesis
- Gonadal disorder
- Gonadal dysgenesis
- Gonadal teratoma
- Gonadoblastoma
- Gonadotropin-dependent precocious puberty
- Gonadotropin-independent precocious puberty
- Gonadotropin-producing adenoma
- Gonadotropin-resistant ovary syndrome
- Gonococcal conjunctivitis
- Gonococcal urethritis
- Gonorrhea
- Grade I vesicoureteral reflux
- Grade ii vesicoureteral reflux
- Grade iii vesicoureteral reflux
- Grade iv vesicoureteral reflux
- Grade v vesicoureteral reflux
- Graft versus host disease
- Gram
- Grandparent visitation
- Granuloma
- Granulomatosis with polyangiitis
- Granulosa cell tumor
- Grasp reflex
- Graves disease
- Gravida
- Gray baby syndrome
- Gray platelet syndrome
- Gray's Anatomy
- Great blood vessel
- Great vessels abnormality
- Green fetal membranes
- Gross abruption
- Gross hematuria
- Gross motor delay
- Gross motor skill#Learning to walk
- Gross total resection
- Group b streptococcal infection, early-onset
- Group b streptococcal infection, late-onset
- Group b streptococcal infection
- Group b streptococcus risk status
- Growth failure of unknown etiology
- Growth failure
- Growth hormone and prolactin-producing adenoma
- Growth hormone deficiency
- Growth hormone excess
- Growth hormone insensitivity syndromes
- Growth hormone neurosecretory dysfunction
- Growth hormone-producing adenoma
- Guillain-barre syndrome
- Gustatory hallucination
- Gynecologic surgical procedure
- Gynecomastia
- H1n1 influenza
- Haberman Feeder
- Haemophilus influenzae b vaccine
- Hair tourniquet
- Hallucination
- Hand, foot, and mouth disease
- Hantavirus nephropathy
- Hantavirus pulmonary syndrome
- Haploidentical donor
- Harlequin ichthyosis
- Harlequin reaction
- Hartnup disease
- Hashimoto thyroiditis
- Hashitoxicosis
- Head circumference
- Head injury
- Headache
- Health Encyclopedia
- Health assessment questionnaire
- Health encyclopedia
- Health topics
- Health
- Healthcare provider directory
- Hearing loss
- Heart block
- Heart disorder
- Heart failure
- Heart murmur
- Heart rate score
- Heart rate
- Heart rhythm
- Heart valve regurgitation
- Heartburn
- Heavy-metal-induced nephropathy
- Heel to ear measurement
- Hellp syndrome
- Hemangioendothelioma
- Hemangioma
- Hematemesis
- Hematochezia
- Hematologic disorder
- Hematology test
- Hematoma
- Hematopoietic stem cell transplantation
- Hematopoietic system finding
- Hematuria
- Hemianopsia
- Hemicrania continua
- Hemihypertrophy
- Hemimelia
- Hemiparesis
- Hemochromatosis
- Hemodialysis catheter infection
- Hemodialysis catheter-associated bacteremia
- Hemodialysis catheter
- Hemoglobin a measurement
- Hemoglobin a to total hemoglobin ratio measurement
- Hemoglobin a1c increased
- Hemoglobin a2 measurement
- Hemoglobin a2 to total hemoglobin ratio measurement
- Hemoglobin barts
- Hemoglobin c disease
- Hemoglobin c to total hemoglobin ratio measurement
- Hemoglobin d disease
- Hemoglobin decreased
- Hemoglobin e disease
- Hemoglobin h disease
- Hemoglobin measurement
- Hemoglobin s to total hemoglobin ratio measurement
- Hemoglobin sc disease
- Hemoglobin trait
- Hemoglobin variant measurement
- Hemoglobinopathy
- Hemoglobinuria
- Hemolysis
- Hemolytic anemia due to erythrocyte membrane defect
- Hemolytic anemia
- Hemolytic disease of the newborn
- Hemolytic uremic syndrome
- Hemopericardium
- Hemophilia a
- Hemophilia b
- Hemophilia
- Hemoptysis
- Hemorrhage
- Hemorrhagic cerebrovascular accident
- Hemorrhagic cystitis
- Hemorrhagic disease of newborn
- Hemorrhoid
- Hemosiderin in decidua basalis
- Hemosiderin in decidua parietalis
- Hemosiderin in intervillous thrombus
- Hemothorax
- Henoch-schönlein purpura nephritis
- Henoch-schönlein purpura
- Heparin-induced thrombocytopenia
- Hepatic arteriovenous malformation
- Hepatic mass
- Hepatitis a infection
- Hepatitis a vaccine
- Hepatitis b infection
- Hepatitis b vaccine
- Hepatitis
- Hepatoblastoma with pure fetal epithelial differentiation
- Hepatoblastoma
- Hepatocellular liver injury
- Hepatocyte nuclear factor 1-alpha hyperinsulinism
- Hepatocyte nuclear factor 1-alpha-associated monogenic diabetes
- Hepatocyte nuclear factor 1-beta-associated monogenic diabetes
- Hepatocyte nuclear factor 4-alpha associated monogenic diabetes
- Hepatocyte nuclear factor 4-alpha hyperinsulinism
- Hepatorenal syndrome
- Hereditary coagulation factor deficiency
- Hereditary connective tissue disorder
- Hereditary elliptocytosis
- Hereditary factor I deficiency
- Hereditary factor ii deficiency
- Hereditary factor iii deficiency
- Hereditary factor v deficiency
- Hereditary factor vii deficiency
- Hereditary factor x deficiency
- Hereditary factor xi deficiency disease
- Hereditary factor xii deficiency
- Hereditary factor xiii deficiency
- Hereditary fructose intolerance
- Hereditary hemolytic anemia
- Hereditary hypophosphatemic rickets with hypercalciuria
- Hereditary neoplastic syndrome
- Hereditary orotic aciduria
- Hereditary pyropoikilocytosis
- Hereditary sideroblastic anemia
- Hereditary spherocytosis
- Hermansky-pudlak syndrome
- Hernia
- Herpetic whitlow
- Heteronymous visual field defect
- Heterophyiasis
- Heterotaxy syndrome with asplenia
- Heterotaxy syndrome with polysplenia
- Heterotaxy syndrome
- Heterotaxy
- Hexokinase deficiency
- Hexose-6-phosphate dehydrogenase deficiency
- Hiatal hernia
- Hiccup
- Hidradenitis suppurativa
- Hidradenitis
- High chair
- High molecular weight kininogen deficiency
- High pitched cry
- High test reference range
- Hip dislocation
- Hirschsprung disease
- Hirsutism
- Histamine-2 receptor antagonist
- Histiocytosis
- Histologic chorioamnionitis
- Histoplasmosis
- Hiv infection
- Hiv-associated nephropathy
- Hmg-coa lyase deficiency
- Hodgkin lymphoma
- Holocarboxylase synthetase deficiency
- Holoprosencephaly
- Homicidal ideation
- Homocystinuria
- Homonymous visual field defect
- Hookworm infection
- Hormone measurement
- Horner syndrome
- Horseshoe kidney
- Human chorionic gonadotropin measurement
- Human leukocyte antigen sensitization
- Human milk banking in North America
- Human papilloma virus vaccine
- Human papillomavirus-16
- Human papillomavirus-18
- Human papillomavirus
- Humerus fracture
- Hutch diverticulum
- Hydatidiform mole
- Hydranencephaly
- Hydroa vacciniforme-like lymphoma
- Hydrocephalus
- Hydronephrosis
- Hydrops fetalis
- Hydrothorax
- Hydroureter
- Hyperactivity
- Hyperacusis
- Hyperacute allograft rejection
- Hyperaldosteronemia
- Hyperaldosteronism
- Hyperalgesia
- Hyperammonemia
- Hyperamylasemia
- Hyperandrogenism, insulin resistance, acanthosis nigricans syndrome
- Hyperandrogenism
- Hyperbilirubinemia
- Hypercalcemia of malignancy
- Hypercalcemia
- Hypercalcuria
- Hypercarbia
- Hypercholesterolemia
- Hypercoiled umbilical cord
- Hypercortisolemia
- Hyperemesis gravidarum
- Hyperesthesia
- Hyperestrogenism
- Hyperfibrinogenemia
- Hyperglucagonemia
- Hyperglycemia
- Hypergonadotropic hypogonadism
- Hyperhidrosis
- Hyperhomocysteinemia
- Hyperinsulinemia
- Hyperinsulinism in the infant of a diabetic mother
- Hyperkalemia
- Hyperkalemic mineralocorticoid resistance
- Hyperkinesia
- Hyperlactemia
- Hyperlipasemia
- Hypermagnesemia
- Hypernatremia
- Hypernatremic dehydration
- Hyperparathyroidism-jaw tumor syndrome
- Hyperparathyroidism
- Hyperphagia
- Hyperphosphatemia
- Hyperphosphatemic familial tumoral calcinosis
- Hyperpigmentation
- Hyperprogesteronism
- Hyperprolactinemia
- Hyperpyrexia
- Hyperreninemic hypoaldosteronism
- Hypersensitivity reaction
- Hypersexualism
- Hypersomnia
- Hypertension
- Hyperthermia
- Hyperthyroidism
- Hyperthyroxinemia
- Hypertonia
- Hypertrichosis
- Hypertriglyceridemia
- Hypertrophic pyloric stenosis
- Hypertrophic scar
- Hyperuricemia
- Hyperventilation
- Hypervolemia
- Hyphema
- Hypoalbuminemia
- Hypocalcemia
- Hypochondroplasia
- Hypochromic anemia
- Hypocitraturia
- Hypocoiled umbilical cord
- Hypocortisolemia
- Hypoesthesia
- Hypogalactia
- Hypogeusia
- Hypoglycemia
- Hypogonadism
- Hypogonadotropic hypogonadism with adrenal hypoplasia congenita
- Hypogonadotropic hypogonadism with anosmia
- Hypogonadotropic hypogonadism
- Hypohidrosis
- Hypokalemia
- Hypokinesia
- Hypomagnesemia
- Hypomanic mood
- Hyponatremia
- Hyponatremic mineralocorticoid resistance due to mineralocorticoid receptor defect
- Hypoparathyroidism
- Hypophagia
- Hypophonia
- Hypophosphatasia
- Hypophosphatemia
- Hypophosphatemic rickets
- Hypophysitis
- Hypopigmentation
- Hypopituitarism
- Hypoplasia
- Hypoplastic left heart syndrome
- Hypoplastic right heart syndrome
- Hypoprogesteronism
- Hypopyon
- Hyporeninemic hypoaldosteronism
- Hyposmia
- Hypospadias
- Hypotension
- Hypothalamic hamartoma
- Hypothalamic hypothyroidism
- Hypothermia
- Hypothyroid goiter
- Hypothyroidism
- Hypothyroxinemia
- Hypotonia
- Hypotonic cerebral palsy
- Hypotonic-hyporesponsive episode
- Hypoventilation
- Hypovolemia
- Hypoxemia
- Hypoxia
- Hypoxic ischemic encephalopathy
- Hysterotomy abortion
- Iatrogenic botulism
- Iatrogenic central hypothyroidism
- Iatrogenic contrasexual pubertal development
- Iatrogenic cushing syndrome
- Iatrogenic growth failure
- Iatrogenic hypoparathyroidism
- Iatrogenic obesity
- Iatrogenic primary hypothyroidism
- Ichthyosis
- Identification
- Idiopathic 46,xy differences of sex development
- Idiopathic aplastic aplasia
- Idiopathic central precocious puberty
- Idiopathic crescentic glomerulonephritis
- Idiopathic inflammatory myopathy
- Idiopathic isolated growth hormone deficiency
- Idiopathic ketotic hypoglycemia
- Idiopathic membranous glomerulopathy
- Idiopathic nephrotic syndrome
- Idiopathic precocious puberty
- Idiopathic renal papillary necrosis
- Idiopathic retroperitoneal fibrosis
- Idiopathic short stature
- Idiopathic tall stature
- Iga nephropathy, familial
- Iga nephropathy, infection-associated
- Iga nephropathy, liver disease-associated
- Iga nephropathy
- Igm - associated nephropathy
- Ileal atresia
- Ileal band
- Ileal perforation
- Ileal web
- Ileostomy site
- Ileus
- Image identifier
- Image syndrome
- Imaging information
- Immature granulocytes in peripheral blood increased
- Immature myeloid cells increased in bone marrow
- Immature retinal vasculature in retinal anatomic zone 1
- Immature retinal vasculature in retinal anatomic zone 2
- Immature retinal vasculature in retinal anatomic zone 3
- Immature retinal vasculature
- Immature retinopathy of prematurity
- Immune complex mediated membranoproliferative glomerulonephritis
- Immune dysregulation, polyendocrinopathy, and enteropathy x-linked syndrome
- Immune globulin
- Immune hemolytic anemia
- Immune hydrops fetalis
- Immune system disorder
- Immune thrombocytopenia
- Immune thrombocytopenic purpura
- Immune-mediated coagulopathy
- Immunization
- Immunocompromised
- Immunodeficiency
- Immunoglobulin superfamily member 1 deficiency syndrome
- Impaired balance
- Impaired judgement
- Imperforate anus
- Impetigo
- Impulsivity
- In utero bowel perforation
- In-utero drug withdrawal
- Inactivated poliovirus vaccine
- Inactivated vaccine
- Inactivating thyroid stimulating hormone receptor gene mutation
- Incarcerated inguinal hernia
- Inch
- Incident nephrotic syndrome
- Inclusion body myositis
- Incomplete abortion
- Incomplete maternal surface of placenta
- Incongruent visual field defect
- Incontinent epispadias
- Incontinentia pigmenti
- Increased bone density
- Increased creatinine
- Increased drug level
- Increased energy
- Increased libido
- Increased placental syncytial knots
- Increased respiratory secretion
- Indicated cesarean delivery
- Indicated preterm birth
- Indicator
- Indirect inguinal hernia
- Indirect maternal death
- Indirect transmission
- Induced abortion
- Induction of labor
- Induration
- Indwelling urinary catheter
- Ineffective hematopoiesis
- Infancy
- Infant acute lymphoblastic leukemia with mll gene rearrangement
- Infant acute lymphoblastic leukemia without mll gene rearrangement
- Infant acute lymphoblastic leukemia
- Infant bathing
- Infant botulism
- Infant cognitive development
- Infant ear piercing
- Infant failure to thrive
- Infant food safety
- Infant formula intolerance
- Infant formula
- Infant irritability
- Infant leukemia
- Infant massage
- Infant nutrition
- Infant of diabetic mother
- Infant reflex
- Infant respiratory distress syndrome
- Infant visual development
- Infant
- Infantile cortical hyperostosis
- Infantile fibrosarcoma
- Infantile pyknocytosis
- Infantile spasms
- Infarct
- Infection
- Infectious conjunctivitis
- Infectious disorder
- Infectious encephalitis
- Infectious hidradenitis
- Infectious keratitis
- Infectious meningitis
- Infectious meningoencephalitis
- Infectious mononucleosis
- Infectious otitis externa
- Infectious rhinitis
- Infective endocarditis
- Inferior vena cava occlusion
- Inferior vena cava stenosis
- Inflammatory bowel disease
- Influenza vaccination
- Influenza
- Infundibular stenosis
- Inguinal hernia
- Inherited color blindness
- Injury
- Inner restlessness
- Inr increased
- Insomnia
- Insufficient breast milk syndrome
- Insulin growth factor I deficiency
- Insulin growth factor I resistance
- Insulin receptor mutation - associated insulin resistance syndromes
- Insulin resistance syndrome
- Insulin resistance
- Insulin resistant diabetes mellitus with acanthosis nigricans and hyperandrogenism
- Insulinoma
- Integumentary system finding
- Intellectual disability
- Intentional trauma
- Intercostal retractions
- Interferon-gamma release assay
- Intermediate uveitis
- Intermittent auscultation
- Intermittent fetal heart rate deceleration
- Internal fetal heart rate monitoring
- Internal nare
- Internal strabismus
- International league of associations for rheumatology classification criteria for juvenile idiopathic arthritis
- International myositis assessment and clinical studies group
- Interrupted aortic arch
- Intervention or procedure
- Intervillous thrombus
- Intestinal duplication
- Intestinal fistula
- Intestinal malrotation
- Intestinal perforation
- Intestinal stricture
- Intestinal volvulus
- Intra-abdominal abscess
- Intra-abdominal hemangioma
- Intraarticular corticosteroid
- Intracranial aneurysm
- Intracranial hemorrhage related to birth
- Intracranial hemorrhage
- Intracranial laceration related to birth
- Intramuscular route of administration
- Intraocular foreign body
- Intraocular infection
- Intraocular lens dislocation
- Intraocular pressure rise
- Intraocular retinoblastoma
- Intrapartum fetal stimulation
- Intrapartum pyrexia
- Intrapartum shock
- Intrapartum stillbirth
- Intrapartum uterine rupture
- Intrauterine cordocentesis
- Intrauterine resuscitation
- Intravenous immunoglobulin
- Intravenous route of administration
- Intraventricular hemorrhage of prematurity
- Intraventricular hemorrhage related to birth
- Intraventricular hemorrhage with parenchymal hemorrhage of newborn
- Intraventricular hemorrhage
- Intravesical ureterocele
- Intrusive thought
- Intussusception
- Invasive candidiasis
- Invasive hydatidiform mole
- Invasive listeriosis
- Iodide transport defect
- Iodine deficiency hypothyroidism
- Iridodialysis
- Iron overload
- Iron-deficiency anemia
- Irregular respiration
- Irritability
- Irritable bowel syndrome
- Ischemic necrosis
- Ischemic nephropathy
- Isolated follicle stimulating hormone deficiency
- Isolated glucocorticoid deficiency
- Isolated non-pigmented micronodular adrenal hyperplasia
- Isovaleric acidemia
- Jaundice
- Jejunal atresia
- Jejunal band
- Jejunal web
- Jejunostomy site
- Jod-basedow
- Joint effusion
- Joint stiffness
- Junctional ectopic tachycardia
- Juvenile arthritis disease activity score
- Juvenile breast papillomatosis
- Juvenile dermatomyositis sine myositis
- Juvenile dermatomyositis
- Juvenile idiopathic arthritis
- Juvenile localized scleroderma
- Juvenile myelomonocytic leukemia
- Juvenile paget disease
- Juvenile pilocytic astrocytoma
- Juvenile polymyositis
- Juvenile primary fibromyalgia syndrome
- Juvenile psoriatic arthritis
- Juvenile spondyloarthritis disease activity index
- Juvenile spondyloarthritis
- Juvenile systemic sclerosis
- Juvenile type granulosa cell tumor
- Juvenile type ovarian granulosa cell tumor
- Juvenile type testicular granulosa cell tumor
- Juvenile xanthogranuloma
- K atp associated transient neonatal diabetes mellitus
- K atp channel-associated diabetes mellitus
- K atp permanent neonatal diabetes
- Kabuki syndrome
- Kangaroo care
- Karyotype
- Katp-associated hyperinsulinism
- Kawasaki disease
- Kearns-sayre syndrome
- Keloid
- Kenny-caffey syndrome type 1
- Kenny-caffey syndrome type 2
- Kenny-caffey syndrome
- Keratitis
- Kernicterus due to isoimmunization
- Kernicterus
- Ketonuria
- Ketotic hypoglycemia
- Kidney allograft thrombosis
- Kidney disease
- Kidney impairment
- Kidney stone
- Kidney tumor
- Kir6.2-associated diabetes mellitus
- Klinefelter syndrome
- Klippel-feil sequence
- Klippel-trenaunay-weber syndrome
- Klumpke's palsy
- Krabbe disease
- Kyphosis
- Labial fusion
- Labor after cesarean
- Labor complication
- Labor
- Laboratory procedure
- Laboratory test result
- Labored breathing
- Labyrinthitis
- Laceration
- Lack of adrenarche
- Lacrimal mucocele
- Lacrimal system disorder
- Lactation suppression
- Lactic acidosis
- Ladd band
- Lamellar laceration of the globe
- Langer type mesomelic dysplasia
- Langerhans cell histiocytosis
- Language disorder
- Lanugo
- Large for gestational age
- Large intestine atresia
- Larger axis of placenta
- Larnygeotracheoesophageal cleft
- Laron syndrome
- Laryngeal agenesis
- Laryngeal atresia
- Laryngeal stenosis
- Laryngeal tube
- Laryngeal web
- Laryngitis
- Laryngomalacia
- Laryngospasm
- Lassa fever
- Lassitude
- Lasso-o measuring tape
- Last menstrual period
- Last screening
- Late adolescence
- Late disseminated lyme disease
- Late fetal death
- Late fetal heart rate deceleration
- Late latent syphilis
- Late neonatal mortality
- Late postpartum hemorrhage
- Late preterm birth
- Late preterm infant
- Late prosthetic valve endocarditis
- Late relapse of acute lymphoblastic leukemia
- Late relapse
- Late term birth
- Latent phase of labor
- Latent syphilis
- Leakage of amniotic fluid
- Learning disorder
- Left ear
- Left ventricular dysfunction
- Left ventricular outflow tract obstruction
- Legionella pneumonia
- Legionellosis
- Leigh disease
- Leishmaniasis
- Length
- Lennox-gastaut syndrome
- Leopard syndrome
- Leprosy
- Leptin deficiency
- Leptin receptor deficiency
- Leptospirosis nephropathy
- Leri-weill syndrome
- Lethargy
- Leukemia
- Leukemoid reaction of the newborn
- Leukemoid reaction
- Leukocytosis
- Leukoderma
- Leukonychia
- Leukopenia
- Leukoplakia
- Levo-transposition of the great vessels
- Leydig cell tumor
- Lichenification
- Lichenoid drug eruption
- Lid retraction
- Liddle syndrome
- Life stage
- Limited cutaneous systemic sclerosis
- Linear scleroderma
- Lingual thyroid gland
- Lipid metabolism disorder
- Lipodystrophy
- Lipoma
- Lissencephaly
- List of hospitals
- List of patient cases
- Lithium - induced nephropathy
- Lithium-induced birth defects
- Live attenuated influenza vaccine
- Live birth
- Liver abscess
- Local anesthesia procedure
- Localized corticosteroid
- Localized scleroderma
- Loiasis
- Long qt syndrome
- Long-chain acyl-coa dehydrogenase deficiency
- Loose stool
- Lordosis
- Loss of consciousness
- Louse-borne relapsing fever
- Low anorectal malformation
- Low birth weight
- Low blood oxygen saturation
- Low complement
- Low natural killer cell activity
- Low t3 syndrome
- Low test reference range
- Low vision
- Low weight gain in pregnancy
- Low-lying placenta
- Lumbar meningocele
- Lumbar myelocele
- Lumbar myelomeningocele
- Lung disorder
- Lung overinflation
- Lupus anti-coagulant antibody
- Lupus anticoagulant disorder
- Lupus erythematosus tumidus
- Lupus erythematosus
- Lupus flare
- Lupus glomerulonephritis
- Lupus headache
- Lupus panniculitis
- Luteinizing hormone deficiency
- Lyme arthritis
- Lyme disease
- Lymphadenitis
- Lymphadenopathy
- Lymphangioma
- Lymphatic filariasis
- Lymphocytic neurohypophysitis
- Lymphocytopenia
- Lymphocytosis
- Lymphoma
- Lysosomal acid lipase deficiency
- Lysosomal storage disorder
- Macrocephaly
- Macrocytic anemia
- Macronodular adrenal hyperplasia
- Macrophage activation syndrome
- Macropsia
- Macrosomia
- Macular edema
- Macular rash
- Macule
- Magnesium ammonium phosphate urolithiasis
- Maiden name
- Majeed syndrome
- Major depressive episode with peripartum onset
- Malabsorption syndrome
- Malabsorption
- Malaise
- Malar rash
- Malaria
- Male circumcision
- Male reproductive system disorder
- Male
- Malignant brain tumor
- Malignant childhood central nervous system neoplasm
- Malignant hypertensive nephropathy
- Malignant hyperthermia
- Malunion
- Manic mood
- Mannosidosis
- Mantoux tuberculin skin test
- Manual fetal rotation
- Manual muscle testing
- Maple syrup urine disease
- Marburg hemorrhagic fever
- Marfan syndrome
- Marginal cord insertion
- Marginal insertion of fetal membranes
- Marked baseline fetal heart rate variability
- Mass
- Mastitis
- Mastoiditis
- Matched related donor
- Matched unrelated donor
- Maternal diabetes and deafness syndrome
- Maternal hypotension
- Maternal life stage
- Maternal mortality
- Maternal postnatal stage
- Maternal preconception stage
- Maternal prenatal stage
- Maternal proteinuria
- Maternal uniparental disomy chromosome 14 syndrome
- Maternal weight gain in pregnancy
- Maturation
- Mauriac syndrome
- May-hegglin anomaly
- Mayer-rokitansky-kuster-hauser syndrome
- Mccune albright syndrome
- Measles/mumps/rubella vaccine
- Measles
- Measurement of hemoglobin c
- Meatal stenosis
- Meckel's diverticulum
- Meckel-gruber syndrome
- Meconium aspiration syndrome
- Meconium ileus
- Meconium peritonitis
- Meconium plug syndrome
- Meconium stained amniotic fluid
- Meconium
- Mediastinal mass
- Mediastinitis
- Medical advice
- Medical device dislodged
- Medical device failure
- Medical device malfunction
- Medical device misplaced
- Medical record number
- Medication administered at birth
- Medium-chain acyl-coa dehydrogenase deficiency
- Medullary cystic kidney disease type I
- Medullary cystic kidney disease type ii
- Medullary sponge kidney
- Medullary thyroid carcinoma
- Medulloblastoma
- Medulloepithelioma
- Megacalycosis
- Megacystis - megaureter
- Megaloblastic anemia 1
- Megaloblastic anemia
- Megaureter
- Melanocortin 4 receptor deficiency
- Melanocortin pathway defects
- Melanoma
- Melasma
- Melena neonatorum
- Melena
- Melioidosis
- Membranoproliferative glomerulonephritis type 3 (aq)
- Membranoproliferative glomerulonephritis
- Membranous lupus nephritis
- Membranous nephropathy - autoimmune disorder associated
- Membranous nephropathy - drug associated
- Membranous nephropathy - idiopathic
- Membranous nephropathy - infection associated
- Membranous nephropathy - nep induced
- Membranous nephropathy - pla2r induced
- Membranous nephropathy - secondary
- Membranous nephropathy - thsd7a induced
- Membranous nephropathy
- Meningioma
- Meningismus
- Meningitis
- Meningococcal conjugate vaccine mcv4
- Meningococcal polysaccharide vaccine mpsv4
- Meningoencephalitis
- Menkes disease
- Menorrhagia
- Menstrual problem
- Mental and behavioral signs and symptoms
- Mental development index
- Mental retardation
- Mental scale
- Mesangial proliferative glomerulonephritis
- Mesenteric abscess
- Mesomelic dysplasias
- Metabolic acidosis
- Metabolic alkalosis
- Metabolic bone disease of prematurity
- Metabolic bone disease
- Metabolic disease
- Metabolic myopathy
- Metagonimiasis
- Metaphyseal chondrodysplasia, jansen type
- Metastatic childhood soft tissue sarcoma
- Methemoglobin reductase deficiency
- Methemoglobinemia
- Methicillin-resistant staphylococcus aureus infection
- Methicillin-resistant staphylococcus aureus pneumonia
- Methylcrotonyl-coa carboxylase deficiency
- Methylmalonic acidemia
- Mevalonate kinase deficiency
- Microbe
- Microcephaly
- Microcolon
- Microcystic renal disease
- Microcytic anemia
- Micrognathism
- Microgyria
- Microinternational unit per milliliter
- Micronodular adrenal hyperplasia
- Microphthalmos
- Micropsia
- Microscopic polyangiitis
- Microsporidiosis
- Middle childhood
- Middle east respiratory syndrome
- Migraine with aura
- Migraine without aura
- Migraine-triggered seizure
- Migraine
- Migrainous infarction
- Migratory arthritis
- Mild bronchopulmonary dysplasia
- Milia
- Miliaria
- Milligram per deciliter
- Millimole per liter
- Miniature adult form of ahc
- Minimal baseline fetal heart rate variability
- Minimal change disease
- Mismatched unrelated donor
- Missed abortion
- Mitochondrial diabetes
- Mitochondrial encephalomyopathy, lactic acidosis and stroke
- Mitochondrial enzyme deficiency
- Mitochondrial hydroxyacyl-coenzyme a dehydrogenase hyperinsulinism
- Mitochondrial myopathy
- Mitochondrial trifunctional protein deficiency
- Mitochondrial uncoupling protein 2 hyperinsulinism
- Mitral valve atresia
- Mitral valve regurgitation
- Mitral valve stenosis
- Mixed cerebral palsy
- Mixed congenital mesoblastic nephroma
- Mixed connective tissue disease
- Mixed epithelial and mesenchymal hepatoblastoma
- Mixed germ cell-sex cord-stromal tumor
- Mixed hearing loss
- Mixed morphea
- Mixed phenotype acute leukemia
- Mixed somatolactotrope adenoma
- Mll gene rearrangement
- Mmih syndrome
- Mobius syndrome
- Modality
- Mode of transmission
- Moderate baseline variability
- Moderate bronchopulmonary dysplasia
- Molar ratio
- Monkeypox
- Monocarboxylate transporter 1 hyperinsulinism
- Monocarboxylate transporter 8 deficiency
- Monochorionic diamniotic twin pregnancy
- Monochorionic monoamniotic twin pregnancy
- Monocular diplopia
- Monocytopenia
- Monocytosis
- Monogenic diabetes
- Monogenic hyperinsulinism
- Monogenic obesity
- Monosomy 13q syndrome
- Mood lability
- Moro reflex
- Mother
- Motor deficits
- Motor development
- Motor developmental delay
- Motor manifestations
- Motor restlessness
- Motor stereotypies
- Motor tic
- Mottled color of placental parenchyma
- Mottling
- Movement disorders
- Movement of lip corners
- Mtor inhibitor - induced nephropathy
- Muckle-wells syndrome
- Mucocutaneous candidiasis
- Mucopolysaccharidosis
- Mucormycosis
- Mucosal ulcer
- Mucositis
- Mulibrey nanism
- Mullerian inhibiting factor deficiency
- Mullerian-renal-cervical spine syndrome
- Multi-organ failure
- Multi-organ involvement
- Multicystic dysplastic kidney
- Multidrug-resistant mycobacterium tuberculosis
- Multidrug-resistant tuberculosis
- Multifocal multisystem langerhans cell histiocytosis
- Multifocal unisystem langerhans cell histiocytosis
- Multilobate placenta
- Multinodular adrenal hyperplasia
- Multinodular goiter
- Multiple endocrine neoplasia syndrome(s)
- Multiple endocrine neoplasia type 1
- Multiple endocrine neoplasia type 2a
- Multiple endocrine neoplasia type 2b
- Multiple gestation
- Multiple sclerosis
- Mumps
- Muscle contraction
- Muscle cramping
- Muscle rigidity
- Muscle stiffness
- Muscle tone score
- Muscle weakness
- Muscular dystrophy
- Musculoskeletal chest pain
- Musculoskeletal finding
- Musculoskeletal system disorder
- Myalgia
- Myasthenia gravis
- Mycoplasmal pneumonia
- Myelitis
- Myeloablative conditioning
- Myelocele
- Myelodysplastic syndrome
- Myeloid sarcoma
- Myiasis
- Myocardial infarction
- Myocarditis
- Myoclonic jerk
- Myoclonus
- Myoglobinuria
- Myopathy
- Myositis activities profile
- Myositis damage index
- Myositis disease activity assessment tool
- Myositis
- Myotonic disorder
- Myotonic dystrophy 1
- Myotonic dystrophy 2
- Myotonic dystrophy
- Nadh dehydrogenase deficiency
- Nail-patella syndrome
- Nalp12-associated hereditary periodic fever syndrome
- Nanny
- Nanogram per deciliter
- Nasal congestion
- Nasal endotracheal tube
- Nasal flaring
- Nasal route of administration
- Nasoduodenal tube
- Nasogastric tube
- Nasojejunal tube
- Nasopharyngitis
- Native valve endocarditis
- Natural birth
- Nausea
- Necrotizing enterocolitis totalis
- Necrotizing enterocolitis
- Necrotizing fasciitis
- Necrotizing funisitis
- Negative group b streptococcus risk status
- Neisseria meningitidis
- Neonatal abstinence syndrome assessment
- Neonatal abstinence syndrome
- Neonatal acrocyanosis
- Neonatal adrenoleukodystrophy
- Neonatal alloimmune thrombocytopenia
- Neonatal aspiration of amniotic fluid
- Neonatal aspiration syndrome
- Neonatal candidiasis
- Neonatal conjunctivitis
- Neonatal dacryocystitis
- Neonatal death
- Neonatal diabetes mellitus
- Neonatal disorder
- Neonatal disseminated intravascular coagulation
- Neonatal drug withdrawal
- Neonatal encephalopathy
- Neonatal graves disease
- Neonatal hepatitis
- Neonatal herpes simplex infection
- Neonatal hyperbilirubinemia
- Neonatal hyperglycemia
- Neonatal hypoglycemia
- Neonatal hypoxic ischemic encephalopathy
- Neonatal infectious disorder
- Neonatal jaundice
- Neonatal listeriosis
- Neonatal lupus erythematosus
- Neonatal neutropenia
- Neonatal opiate withdrawal syndrome
- Neonatal polycythemia
- Neonatal respiratory system disorder
- Neonatal seizure
- Neonatal sepsis, early-onset
- Neonatal sepsis, late-onset
- Neonatal sepsis
- Neonatal severe primary hyperparathyroidism
- Neonatal spell
- Neonatal tetanus
- Neonatal thrombocytopenia
- Neonatal thyrotoxicosis
- Neonatal vaginal discharge
- Neonatal withdrawal
- Neonatal-onset multisystem inflammatory disease
- Neoplasm
- Nephritic syndrome
- Nephritis
- Nephroblastoma
- Nephrocalcinosis
- Nephrogenic diabetes insipidus
- Nephrogenic systemic fibrosis
- Nephronophthisis
- Nephropathy associated with rhabdomyolysis
- Nephropathy due to aminoglycosides
- Nephropathy due to amphotericin
- Nephropathy due to analgesic drugs
- Nephropathy due to ciclosporin
- Nephropathy due to cisplatin
- Nephropathy due to tacrolimus
- Nephropathy
- Nephrostomy site
- Nephrotic range proteinuria
- Nephrotic syndrome - actn4 associated
- Nephrotic syndrome - adck4 associated
- Nephrotic syndrome - anln associated
- Nephrotic syndrome - arhgap24 associated
- Nephrotic syndrome - arhgdia associated
- Nephrotic syndrome - cd2ap associated
- Nephrotic syndrome - cfh associated
- Nephrotic syndrome - coq2 associated
- Nephrotic syndrome - coq6 associated
- Nephrotic syndrome - crb2 associated
- Nephrotic syndrome - cubn associated
- Nephrotic syndrome - cytomegalovirus associated
- Nephrotic syndrome - dgke associated
- Nephrotic syndrome - emp2 associated
- Nephrotic syndrome - epstein-barr virus associated
- Nephrotic syndrome - frequently relapsing
- Nephrotic syndrome - hepatitis c virus associated
- Nephrotic syndrome - human immunodeficiency virus associated
- Nephrotic syndrome - inf2 associated
- Nephrotic syndrome - infection associated
- Nephrotic syndrome - infrequently relapsing
- Nephrotic syndrome - itga3 associated
- Nephrotic syndrome - itgb4 associated
- Nephrotic syndrome - lamb2 associated
- Nephrotic syndrome - lmx1b associated
- Nephrotic syndrome - malaria associated
- Nephrotic syndrome - mefv associated
- Nephrotic syndrome - myo1e associated
- Nephrotic syndrome - neil1 associated
- Nephrotic syndrome - nphs1 associated
- Nephrotic syndrome - nphs2 associated
- Nephrotic syndrome - parvovirus b19 associated
- Nephrotic syndrome - pdss2 associated
- Nephrotic syndrome - plce1 associated
- Nephrotic syndrome - ptpro associated
- Nephrotic syndrome - relapse
- Nephrotic syndrome - scarb2 associated
- Nephrotic syndrome - simian virus 40 associated
- Nephrotic syndrome - smarcal1 associated
- Nephrotic syndrome - syphilis associated
- Nephrotic syndrome - toxoplasmosis associated
- Nephrotic syndrome - trpc6 associated
- Nephrotic syndrome - wt1 associated
- Nephrotic syndrome of childhood - steroid resistant
- Nephrotic syndrome of childhood - steroid sensitive
- Nephrotic syndrome- steroid dependent
- Nephrotic syndrome-remission, partial remission
- Nephrotic syndrome
- Nervous system disorder
- Nervous system finding
- Nervous system neoplasm
- Nesidioblastosis
- Neural tube defect
- Neuralgia
- Neuritis
- Neuroblastoma
- Neurocysticercosis
- Neurodermatitis
- Neurodevelopmental disorder
- Neuroendocrine cell hyperplasia of infancy
- Neuroendocrine tumor
- Neurofibromatosis type 1
- Neurofibromatosis
- Neurogenic bladder
- Neurogenic differentiation factor 1-associated monogenic diabetes
- Neurologic examination
- Neurological screening
- Neuromuscular maturity assessment
- Neuronal migration abnormalities
- Neuropathy
- Neurosyphilis
- Neurotrophic tyrosine kinase, receptor type 2 deficiency
- Neutropenia
- Neutrophilia
- Neutrophilic eccrine hidradenitis
- New daily persistent headache
- New onset diabetes after transplant
- Newborn behavorial examination
- Newborn blood pressure
- Newborn care and safety
- Newborn examination
- Newborn heart rate
- Newborn motor scale
- Newborn or infant finding
- Newborn respiratory rate
- Newborn screening
- Newborn
- Niemann-pick disease
- Night blindness
- Night sweats
- Night terrors
- Nightmare
- No resection
- No
- Nocturia
- Nodular goiter
- Noise-induced hearing loss
- Non-biologic disease-modifying antirheumatic drug
- Non-cesarean uterine surgical scarring
- Non-classic congenital adrenal hyperplasia
- Non-communicating hydrocephalus
- Non-familial idiopathic short stature
- Non-familial idiopathic tall stature
- Non-functioning pituitary gland adenoma
- Non-gonococcal urethritis
- Non-hodgkin lymphoma
- Non-immune hydrops fetalis
- Non-metastatic childhood soft tissue sarcoma
- Non-myeloablative conditioning
- Non-neurogenic neurogenic bladder
- Non-obstructed megaureter
- Non-obstructed non-refluxing megaureter
- Non-rh blood group isoimmunization
- Nonerosive arthritis
- Nonfunctional pituitary macroadenoma
- Nonfunctional pituitary microadenoma
- Nongerminomatous germ cell tumor
- Nonreassuring fetal status
- Nonsteroidal antiinflammatory drug
- Nonunion
- Noonan syndrome
- Normal pupillary response
- Normal reference range
- Normal spontaneous vaginal delivery
- Normocytic anemia
- Nosocomial infection
- Nsaid-induced nephropathy
- Nuchal cord
- Nuchal translucency measurement
- Nulliparous
- Number of centimeters dilated on admission
- Numbness
- Nutrition
- Nutritional calcium deficient rickets
- Nutritional disorder
- Nutritional hypophosphatemic rickets
- Nutritional rickets
- Nutritional vitamin d deficiency rickets
- Nystagmus
- Obesity related glomerulopathy
- Obesity-associated insulin resistance
- Object permanence
- Observation
- Obsessive compulsive disorder
- Obsessive thinking
- Obstetric procedure
- Obstructed megaureter
- Obstructive nephropathy
- Obstructive sleep apnea
- Obstructive ureterocele
- Obstructive uropathy
- Occipital diastasis
- Occult umbilical cord prolapse
- Occupational therapy
- Ocular contusion
- Ocular foreign body
- Ocular hypertension
- Ocular injury
- Oculo-respiratory-syndrome
- Oculocardiac reflex
- Oculocerebrorenal syndrome
- Odontohypophosphatasia
- Oeis syndrome
- Olfactory hallucination
- Oligoarticular arthritis
- Oligoarticular juvenile idiopathic arthritis
- Oligohydramnios
- Oligomeganephronia
- Oligomenorrhea
- Oligospermia
- Oliguria
- Omphalitis
- Omphalocele
- Omphalorrhexis
- Onchocerciasis
- One minute after birth
- Onychodystrophy
- Onycholysis
- Onychomycosis
- Open adoption
- Open angle glaucoma
- Open fracture
- Open globe injury
- Opportunistic infection
- Oppositionality
- Opsoclonus
- Optic disc edema
- Optic nerve hypoplasia
- Optic neuritis
- Optic neuropathy
- Oral candidiasis
- Oral endotracheal tube
- Oral polio vaccine
- Oral rehydration therapy
- Oral route of administration
- Orbital cellulitis
- Orbital contusion
- Orbital fracture
- Orbital muscle entrapment
- Orbital myositis
- Orchitis
- Organic acid metabolism disorder
- Organic growth hormone deficiency
- Organism
- Organismal process
- Ornithine carbamoyltransferase deficiency disease
- Oropharyngeal dysphagia
- Orthostatic hypotension
- Ortolani maneuver
- Osteochondrodysplasia
- Osteoclast-rich osteopetrosis
- Osteogenesis imperfecta type I
- Osteogenesis imperfecta type ii
- Osteogenesis imperfecta type iii
- Osteogenesis imperfecta type iv
- Osteogenesis imperfecta
- Osteoma cutis
- Osteomalacia
- Osteomyelitis
- Osteonecrosis
- Osteopetrosis
- Osteoporosis pseudoglioma syndrome
- Osteoporosis
- Osteosarcoma
- Osteosclerosis
- Ostomy site pain
- Ostomy site
- Other
- Otitis externa
- Otitis media with effusion
- Otitis media
- Otolaryngologic disorder
- Otorrhea
- Ounce
- Ovalocytosis
- Ovarian cyst
- Ovarian disorder
- Ovarian failure
- Ovarian germ cell tumor
- Ovarian gonadoblastoma
- Ovarian granulosa cell tumor
- Ovarian granulosa-stromal tumor
- Ovarian hyperandrogenism
- Ovarian leydig cell tumor
- Ovarian mixed germ cell-sex cord-stromal tumor
- Ovarian pregnancy
- Ovarian sertoli cell tumor
- Ovarian sertoli-leydig cell tumor
- Ovarian sertoli-stromal tumor
- Ovarian sex cord-stromal tumor
- Ovarian stromal-leydig tumor
- Ovarian torsion
- Overlap syndrome
- Oversedation
- Overweight
- Ovotesticular differences of sex development
- Oxygen saturation measurement
- P1 hydronephrosis
- P2 hydronephrosis
- P3 hydronephrosis
- P450 oxidoreductase deficiency
- P450-aromatase deficiency
- Pacifier
- Page kidney
- Pain amplification syndrome
- Pain
- Pallister-hall syndrome
- Pallister-killian syndrome
- Pallor
- Palmar crease examination
- Palmoplantar keratoderma
- Palpable purpura
- Palpitation
- Palsy
- Pancreatitis
- Pancytopenia
- Panhypopituitarism
- Panic disorder with agoraphobia
- Panic disorder without agoraphobia
- Panniculitis
- Pansclerotic morphea
- Panuveitis
- Papillary thyroid carcinoma
- Papilledema
- Papule
- Paracoccidioidomycosis
- Paragonimiasis
- Paralysis
- Paranoia
- Parapharyngeal abscess
- Parasite
- Parasitic infection
- Parasomnia
- Parathyroid hormone resistance
- Parenchymal hemorrhage of newborn
- Parent assessment of overall well-being
- Parent global assessment of disease activity
- Parent
- Parental child abduction
- Parental responsibility (access and custody)
- Parenteral nutrition - associated cholestasis
- Parenteral route of administration
- Parenting plan
- Parenting
- Paresthesia
- Parietal decidual spiral vessel with fibrinoid necrosis-atherosis
- Parity
- Parkinsonism
- Paronychia
- Paronychial inflammation
- Parosmia
- Parotitis
- Partial anomalous pulmonary venous return
- Partial hydatidiform mole
- Partial lipodystrophy
- Partial resection
- Pass
- Patent ductus arteriosus
- Patent urachus
- Paternity fraud
- Paternity law
- Pathogen
- Pathologic av fistula
- Pathological gynecomastia
- Patient assessment of overall well-being
- Patient global assessment of disease activity
- Patient reported outcome
- Patient-reported outcomes measurement information system measures
- Pauci-immune glomerulonephritis - anca negative
- Pauci-immune glomerulonephritis - renal limited
- Pauciarticular juvenile rheumatoid arthritis (aq)
- Pdx1-associated monogenic diabetes
- Pearson syndrome
- Pedialyte
- Pediatric disorder
- Pediatric failure to thrive
- Pediatric glossary of terms expanded
- Pediatric glossary of terms
- Pediatric infectious disease
- Pediatric intervention or procedure
- Pediatric non-congenital ventricular tachycardia
- Pediatric osteoporosis
- Pediatric psychiatric disorder
- Pediatric quality of life inventory
- Pediatric vasculitis activity score
- Pediatric viral infection
- Pediatrics
- Pediculosis
- Peekaboo
- Pelvic abscess
- Pelvic inflammatory disease
- Pelvic kidney
- Pelvic pain
- Pelviureteric junction obstruction
- Pemphigoid gestationis
- Pena-shokeir syndrome
- Pendred syndrome
- Penetrating open globe injury
- Penile agenesis
- Penile chordee
- Penoscrotal transposition
- Pentalogy of cantrell
- Peptic ulcer
- Percutaneous endoscopic tube
- Perforating open globe injury
- Perforation
- Peri-implantational loss
- Pericardial anomaly
- Pericardial effusion
- Pericardial tube
- Pericarditis
- Perihepatic abscess
- Perinatal blood aspiration syndrome
- Perinatal brain injury
- Perinatal central nervous system depression
- Perinatal cyanotic attack
- Perinatal depression
- Perinatal disorder
- Perinatal drug withdrawal
- Perinatal intracranial hemorrhage
- Perinatal intraventricular hemorrhage
- Perinatal jaundice due to inspissated bile syndrome
- Perinatal mortality
- Perinatal respiratory distress
- Perinatal subependymal hemorrhage
- Perinatal-stress induced hyperinsulinism
- Perinephric abscess
- Perinephric hematoma
- Periodic fetal heart rate pattern
- Periodic fever syndrome
- Periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome
- Peripheral blood stem cell transplantation
- Peripheral edema
- Peripheral nervous system disorder
- Peripheral neuropathy
- Peripheral resistance to thyroid hormone
- Peripheral visual field defect
- Peripherally inserted central catheter
- Peritoneal dialysis catheter infection
- Peritoneal dialysis catheter-associated peritonitis
- Peritoneal dialysis catheter
- Peritonitis
- Peritonsillar abscess
- Periventricular hemorrhage of newborn
- Periventricular leukomalacia
- Permanent neonatal diabetes mellitus
- Pernicious anemia
- Peroxisomal disorder
- Persistent cloaca
- Persistent fetal bradycardia
- Persistent fetal tachycardia
- Persistent mullerian duct syndrome type 1
- Persistent mullerian duct syndrome type 2
- Persistent mullerian duct syndrome
- Persistent oligoarticular juvenile idiopathic arthritis
- Persistent pulmonary hypertension of the newborn
- Persistent truncus arteriosus
- Person name
- Person
- Personal information
- Personal medical history
- Pervasive developmental disorder
- Petechiae
- Phakomatosis
- Phantom taste perception
- Phantosmia
- Pharmacologic substance
- Pharyngitis
- Phenylalanine measurement
- Phenylalanine to tyrosine ratio measurement
- Phenylketonuria
- Philadelphia-like acute lymphoblastic leukemia
- Phlebitis
- Phocomelia
- Phonic tic
- Phonophobia
- Phosphoenolpyruvate carboxykinase deficiency
- Phosphoglycerate mutase deficiency
- Photokeratitis
- Photophobia
- Phrenic nerve injury
- Phrenic nerve palsy related to birth
- Phrenic nerve palsy
- Physical dependence
- Physical examination
- Physical maturity assessment
- Physical symmetry
- Physical therapy
- Physician global assessment of disease activity
- Physiologic hyperbilirubinemia
- Pica
- Pierre robin syndrome
- Pierson syndrome
- Pigmentary change of nails
- Pigmentary change of skin
- Pigtail drain
- Pinealoma
- Pineocytoma
- Pituitary abscess
- Pituitary gigantism
- Pituitary gland adenoma
- Pituitary hypoplasia
- Pituitary hypothyroidism
- Pituitary resistance to thyroid hormone
- Pituitary stalk interruption syndrome
- Pituitary stalk lesion
- Pituitary tumor
- Placement
- Placenta accreta
- Placenta increta
- Placenta percreta
- Placenta previa
- Placental abruption
- Placental aromatase deficiency
- Placental disc thickness
- Placental disorder
- Placental fibrinoid deposition
- Placental findings
- Placental hypertrophy
- Placental infarct
- Placental lesion
- Placental mesenchymal dysplasia
- Placental retention
- Placental stromal dusty mineralization
- Placental villous dysmaturity
- Placental villous fibrosis
- Placental villous stromal hemorrhage
- Placental villous stromal-vascular karyorrhexis
- Plague
- Plantar grasp reflex finding
- Plaque
- Plasma kallikrein deficiency
- Plasmapheresis
- Platelet abnormality
- Platelet-type von willebrand disease
- Play (activity)
- Playpen
- Pleocytosis
- Plethoric face
- Pleural effusion
- Pleuritis
- Pleuropulmonary blastoma
- Plurality
- Pneumatosis intestinalis
- Pneumatosis
- Pneumococcal 10-valent conjugate vaccine
- Pneumococcal 13-valent conjugate vaccine
- Pneumococcal 7-valent conjugate vaccine
- Pneumococcal conjugate vaccine
- Pneumococcal polyvalent vaccine
- Pneumocystis pneumonia
- Pneumomediastinum
- Pneumonia
- Pneumonitis
- Pneumopericardium
- Pneumoperitoneum
- Pneumothorax
- Poikiloderma
- Point in time test given
- Poland syndrome
- Polio vaccination
- Poliovirus
- Polyarteritis nodosa
- Polyarticular arthritis
- Polyarticular juvenile idiopathic arthritis, rheumatoid factor negative
- Polyarticular juvenile idiopathic arthritis, rheumatoid factor positive
- Polyarticular juvenile rheumatoid arthritis (aq)
- Polycystic kidney disease
- Polycystic ovary syndrome
- Polycythemia vera
- Polycythemia
- Polydactyly
- Polydipsia
- Polygenic obesity
- Polyhydramnios
- Polymicrogyria
- Polymorphic ventricular tachycardia
- Polymyositis
- Polyostotic fibrous dysplasia
- Polysaccharide vaccine
- Polyuria
- Polyvalent vaccine
- Pontiac fever
- Poor feeding
- Poor sucking reflex
- Poor weight gain
- Popliteal angle measurement
- Porencephalic cyst
- Port site infection
- Port wine stain
- Portal hypertension
- Portal:Medicine
- Positive blood culture
- Positive group b streptococcus risk status
- Positive herpes simplex virus culture
- Positive pseudomonas culture
- Post term birth
- Post term pregnancy
- Post-hemorrhagic hydrocephalus
- Post-herpetic neuralgia
- Post-inflammatory hydrocephalus
- Post-natal death at 16-20 weeks gestation
- Post-pericardiotomy syndrome
- Post-procedural pain
- Post-streptococcal arthritis
- Post-transplant lymphoproliferative disorder
- Post-traumatic stress disorder
- Post-treatment lyme disease syndrome
- Postal code
- Posterior fossa syndrome
- Posterior reversible encephalopathy syndrome
- Posterior urethral valve
- Posterior urethral valves type 1
- Posterior urethral valves type 3
- Posterior uveitis
- Posterior vitreous detatchment
- Postmenstrual age
- Postnasal drip
- Postnatal drug withdrawal
- Postoperative hemorrhage
- Postoperative infection
- Postoperative wound infection
- Postpartum acute renal failure
- Postpartum complication
- Postpartum endometritis
- Postpartum hemorrhage
- Postpartum hysterectomy
- Postpartum obstetric air embolism
- Postpartum obstetric septic embolism
- Postpartum obstetric thromboembolism
- Postpartum pyrexia
- Postpartum shock
- Postpartum thyroiditis
- Postpartum uterine inversion
- Postterm infant
- Potter syndrome
- Pound
- Prader-willi syndrome
- Pre-embryonic loss
- Pre-extensively drug-resistant mycobacterium tuberculosis
- Pre-extensively drug-resistant tuberculosis
- Precipitous birth
- Precocious puberty
- Preeclampsia
- Pregestational diabetes
- Pregnancy complication
- Pregnancy disorder
- Pregnancy finding
- Pregnancy outcome
- Pregnancy with intrauterine device
- Pregnancy
- Prekallikrein deficiency
- Premature adrenarche
- Premature closure of ductus arteriosus
- Premature epiphyseal fusion
- Premature menarche
- Premature rupture of membranes
- Premature thelarche
- Prenatal cocaine exposure
- Prenatal development
- Presbycusis
- Preseptal cellulitis
- Pressured speech
- Presyncope
- Preterm birth
- Preterm infant
- Preterm labor
- Preterm neonatal stage
- Preterm premature rupture of membranes
- Prevalent nephrotic syndrome
- Prevertebral abscess
- Priapism
- Primary adrenal glucocorticoid excess
- Primary adrenal insufficiency
- Primary amenorrhea
- Primary carnitine deficiency
- Primary cesarean birth
- Primary collapsing glomerulopathy
- Primary cough headache
- Primary exertional headache
- Primary fanconi syndrome
- Primary focal segmental glomerulosclerosis
- Primary hyperoxaluria type I
- Primary hyperoxaluria type ii
- Primary hyperoxaluria type iii
- Primary hyperoxaluria
- Primary hyperparathyroidism
- Primary hypersomnia
- Primary hyperthyroidism
- Primary hypoparathyroidism
- Primary hypothyroidism
- Primary malignant liver neoplasm
- Primary ovarian failure
- Primary pigmented nodular adrenal dysplasia
- Primary raynaud phenomenon
- Primary sjogren syndrome
- Primary syphilis
- Primary testicular failure
- Prion disease
- Pro-opiomelanocortin deficiency
- Proctalgia fugax
- Proctitis
- Productive cough
- Progressive diaphyseal dysplasia
- Progressive hemifacial atrophy
- Progressive multifocal leukoencephalopathy
- Progressive osseous heteroplasia
- Prohormone convertase 1 deficiency
- Projectile vomiting
- Prolactin deficiency
- Prolactinoma
- Prolapse
- Prolonged fetal heart rate acceleration
- Prolonged fetal heart rate deceleration
- Prolonged latent phase of labor
- Property or attribute
- Propionic acidemia
- Proprioceptive hallucination
- Proptosis
- Prostatitis
- Prosthetic valve dysfunction
- Prosthetic valve endocarditis
- Protein c deficiency disease
- Protein s deficiency disease
- Proteinuria
- Proton pump inhibitor
- Protozoal infection
- Proximal renal tubular acidosis
- Proximal tubulopathy
- Prune belly syndrome
- Pruritus
- Pseudoaneurysm
- Pseudohypoaldosteronism type 1
- Pseudohypoaldosteronism type 2
- Pseudohypoaldosteronism
- Pseudohypoparathyroidism
- Pseudomenstruation
- Pseudoporphyria
- Pseudostrabismus
- Pseudotumor of kidney
- Psittacosis
- Psoriasiform dermatitis
- Psoriasis
- Psoriatic arthritis
- Psoriatic juvenile idiopathic arthritis
- Psychiatric disorder
- Psychogenic seizure
- Psychogenic tremor
- Psychological dependence
- Psychomotor agitation
- Psychosis
- Pterygium colli
- Ptosis
- Pubertal failure
- Pubertal gynecomastia
- Pulmonary agenesis
- Pulmonary alveolar hemorrhage
- Pulmonary arteriovenous fistula
- Pulmonary edema
- Pulmonary embolism
- Pulmonary fibrosis
- Pulmonary function test decreased
- Pulmonary hemorrhage
- Pulmonary hypertension
- Pulmonary interstitial emphysema
- Pulmonary nodules
- Pulmonary stenosis
- Pulmonary trunk hypoplasia
- Pulmonary valve atresia with intact ventricular septum
- Pulmonary valve atresia with ventricular septal defect
- Pulmonary valve atresia
- Pulmonary vein obstruction
- Pulmonary vein stenosis
- Pulse oximetry
- Pulse rate
- Pupils equal round and reactive to light and accommodation
- Pupils equal round and reactive to light
- Pure red cell aplasia
- Purified protein derivative
- Purpura
- Purulent discharge
- Pustular eruption
- Pustule
- Pycnodysostosis
- Pyelonephritis
- Pyloric stenosis
- Pyogenic arthritis, pyoderma gangrenosum and acne
- Pyogenic granuloma
- Pyomyositis
- Pyonephrosis
- Pyramidal tract syndrome
- Pyrimidine-5'-nucleotidase deficiency
- Pyrogenic reaction
- Pyruvate carboxylase deficiency
- Pyruvate dehydrogenase deficiency
- Pyruvate kinase deficiency
- Pyuria
- Q fever
- Qt prolongation
- Quadriplegia
- Quadruplet pregnancy
- Qualitative concept
- Quantitative concept
- Quantitative muscle testing
- R-r interval
- Rabies
- Rabson-mendenhall syndrome
- Race
- Racing thoughts
- Radial aplasia-thrombocytopenia syndrome
- Radial hypoplasia
- Radiation cystitis
- Radiation damage
- Radiation dermatitis
- Radiation nephropathy
- Radiation recall dermatitis
- Radiculitis
- Radius fracture
- Range
- Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation syndrome
- Rapidly progressive glomerulonephritis
- Rare diseases
- Rat-bite fever
- Rathke cleft cyst
- Raynaud phenomenon
- Reactive airway disease (aq)
- Reactive amniocytes
- Reactive arthritis
- Reactive attachment disorder of infancy or early childhood
- Recombinant viral vaccine
- Rectal prolapse
- Rectal stenosis
- Rectal tube
- Rectal-vesico-vaginal fistula
- Recurrent disease
- Recurrent fetal heart rate deceleration
- Recurrent laryngeal nerve injury
- Recurrent laryngeal nerve palsy
- Recurrent primary malignancy
- Recurrent subsequent malignancy
- Recurrent variable fetal heart rate decelerations
- Red man syndrome
- Red reflex vision test
- Reductase deficiency
- Referral
- Reflex irritability score
- Reflex
- Reflux nephropathy
- Refluxing megaureter
- Refluxing obstructed megaureter
- Refractory cytopenia of childhood
- Refractory disease
- Refusal to bear weight
- Regional anesthesia procedure
- Regression
- Regurgitation
- Remote intervillous thrombus
- Remote placental infarct
- Renal abscess
- Renal agenesis
- Renal artery stenosis
- Renal artery thrombosis
- Renal cell carcinoma
- Renal cell dysplasia
- Renal colic
- Renal coloboma syndrome
- Renal dysplasia due to fetal exposure to ace inhibitor or arb
- Renal failure
- Renal hypertrophy
- Renal infarct
- Renal lymphocele
- Renal osteodystrophy
- Renal parathyroid hormone resistance
- Renal tuberculosis
- Renal tubular acidosis associated with deafness
- Renal tubular acidosis
- Renal vein thrombosis
- Repeat cesarean birth
- Repetitive behaviors
- Reproductive system disorder
- Reproductive system finding
- Residency Program
- Residential telephone number
- Respiratory acidosis
- Respiratory alkalosis
- Respiratory arrest
- Respiratory depression
- Respiratory distress syndrome
- Respiratory distress
- Respiratory failure related to central nervous system disorder
- Respiratory failure related to neuromuscular disorder
- Respiratory failure
- Respiratory rate
- Respiratory syncytial virus infection
- Respiratory system disorder
- Respiratory system finding
- Restless leg syndrome
- Restlessness
- Retching
- Reticulocytopenia
- Retinal detachment
- Retinal disorder
- Retinal examination
- Retinal tear
- Retinitis
- Retinoblastoma
- Retinoic acid syndrome
- Retinopathy of prematurity in retinal anatomic zone 1
- Retinopathy of prematurity in retinal anatomic zone 2
- Retinopathy of prematurity in retinal anatomic zone 3
- Retinopathy of prematurity stage 0
- Retinopathy of prematurity stage 1
- Retinopathy of prematurity stage 2
- Retinopathy of prematurity stage 3
- Retinopathy of prematurity stage 4
- Retinopathy of prematurity stage 5
- Retinopathy of prematurity with plus disease
- Retinopathy of prematurity
- Retinopathy
- Retractile testicle
- Retrobulbar hemorrhage
- Retroperitoneal abscess
- Retropharyngeal abscess
- Retroplacental thrombus
- Rett syndrome
- Reye syndrome
- Rh immune globulin administration
- Rh titer measurement
- Rhabdoid tumor of the kidney
- Rhabdoid tumor
- Rhabdomyolysis
- Rhabdomyoma
- Rhabdomyosarcoma
- Rhegmatogenous retinal detachment
- Rhesus hemolytic disease of the newborn
- Rhesus isoimmunization
- Rheumatic disease
- Rheumatic fever
- Rheumatic heart disease
- Rheumatoid arthritis
- Rheumatoid factor
- Rheumatoid nodule
- Rhinitis
- Rhinorrhea
- Rhinosinusitis
- Rhinovirus infection
- Rhizomelic chondrodysplasia punctata
- Rhizomelic dysplasia
- Rhonchi
- Rib fracture
- Rickets
- Riedel thyroiditis
- Rieger syndrome
- Rift valley fever
- Right aortic arch
- Right atrial thrombus
- Right ear
- Right ventricular dysfunction
- Rigor
- Risk factor assessment
- Rocky mountain spotted fever
- Rooting reflex
- Rosacea
- Roseola infantum
- Rotavirus vaccine
- Rotavirus
- Route of administration
- Rubella immunization
- Rubella screening
- Rubella
- Rubinstein-taybi syndrome
- Rumination
- Rupture of vessel
- Ruptured globe
- Ruptured velamentous vessel
- Russell-silver syndrome
- S-beta thalassemia
- Sacral agenesis
- Sacral fistula
- Sacral meningocele
- Sacral myelocele
- Sacral myelomeningocele
- Sacral sinus
- Sacrococcygeal teratoma
- Sadness
- Saethre-chotzen syndrome
- Salt-wasting 21-hydroxylase deficiency
- Sandifer's syndrome
- Sarcoidosis
- Sarcoma
- Scabies
- Scar
- Scarf sign
- Scarlet fever
- Schistosomiasis nephropathy
- Schistosomiasis
- Schizencephaly
- Scimitar syndrome
- Scleral icterus
- Sclerema neonatorum
- Scleritis
- Scleroderma en coup de sabre
- Scleroderma renal crisis
- Scleroderma
- Sclerosing peritonitis
- Sclerosteosis
- Scoliosis
- Scotoma
- Screaming
- Sebastian syndrome
- Seborrheic dermatitis
- Second degree burn
- Second degree perineal laceration
- Second trimester antepartum hemorrhage
- Secondary amenorrhea
- Secondary collapsing glomerulopathy
- Secondary focal segmental glomerulosclerosis
- Secondary hyperparathyroidism
- Secondary hypogammaglobulinemia
- Secondary parathyroid hormone resistance
- Secondary raynaud phenomenon
- Secondary sjogren syndrome
- Secondary syphilis
- Sedation
- Seizure
- Selective mutism
- Selective reduction of multifetal pregnancy
- Self-injury
- Seminoma
- Sensorineural hearing loss
- Sensory disorder
- Separation anxiety disorder
- Sepsis
- Septic arthritis
- Septic shock
- Septo-optic dysplasia
- Serkal syndrome
- Seroma
- Seronegative
- Serositis
- Serous retinal detachment
- Sertoli cell tumor
- Serum sickness
- Severe acute respiratory syndrome
- Severe aplastic anemia
- Severe bronchopulmonary dysplasia
- Severe combined immunodeficiency
- Severe malaria
- Severe preeclampsia
- Severe sepsis
- Sex chromosome differences of sex development
- Sex cord-stromal tumor
- Sex hormone-binding globulin deficiency
- Sex
- Sexual dysfunction
- Sexually transmitted infection
- Shakiness
- Shock
- Shone syndrome
- Short bowel syndrome
- Short segment hirschsprung's disease
- Short stature
- Short umbilical cord
- Short-term fetal heart rate variability
- Shorter axis of placenta
- Shoulder dystocia
- Shoulder presentation
- Shox deficiency
- Shunt thrombosis
- Sialitis
- Sialorrhea
- Sicca syndrome
- Sick euthyroid syndrome
- Sick newborn
- Sickle beta 0 thalassemia
- Sickle beta plus thalassemia
- Sickle beta thalassemia
- Sickle cell disease
- Sickle cell nephropathy
- Sickle cell trait
- Sickle cell-ss disease
- Sickle cell-thalassemia
- Sideroblastic anemia
- Sign or symptom
- Simple cyst of kidney
- Simple tic
- Simple virilizing 21-hydroxylase deficiency
- Simpson-golabi-behmel syndrome
- Single central incisor syndrome
- Single palmar crease
- Single umbilical artery
- Single ventricle defect
- Sinusitis
- Sinusoidal fetal heart rate pattern
- Sirenomelia
- Site of fetal membrane rupture
- Situs inversus thoracis
- Situs inversus
- Sjogren syndrome
- Skin atrophy
- Skin color score
- Skin disorder
- Skin eschar
- Skin hemangioma
- Skin necrosis
- Skin photosensitivity
- Skin rash
- Skin sloughing
- Skin ulceration
- Skull fracture
- Sleep apnea
- Sleep disorder
- Sleep paralysis
- Sleep related eating disorder
- Sleep
- Slipped capital femoral epiphysis
- Slipped extraocular muscle
- Small cell undifferentiated hepatoblastoma
- Small for gestational age for length
- Small for gestational age for weight and length
- Small for gestational age for weight
- Small for gestational age with failure of catch-up growth
- Small for gestational age
- Small intestine atresia
- Smallpox
- Smith-lemli-opitz syndrome
- Smoking history
- Sneezing
- Snoring
- Social anxiety disorder
- Social history
- Soft tissue sarcoma
- Solitary cyst of kidney
- Solitary multilocular renal cyst
- Somatolactotrope adenoma
- Somatotropin deficiency
- Somnambulism
- Somnolence
- Sotos syndrome
- Southern tick-associated rash illness
- Soy formula
- Spastic cerebral palsy
- Spastic diplegia
- Spastic hemiplegia
- Spastic quadriplegia
- Spasticity
- Specific phobia
- Speech disorder
- Spherocytosis
- Sphincteric ureterocele
- Sphingolipidosis
- Spina bifida cystica
- Spina bifida occulta
- Spina bifida
- Spinal cord infarct related to birth
- Spinal cord infarction
- Spinal cord injury related to birth
- Spinal cord injury
- Spinal cord tumor
- Spinal deformity
- Spinal injury
- Spinal meningocele
- Spinal muscular atrophy
- Spindle cell rhabdomyosarcoma
- Splenic rupture related to birth
- Spondylitis
- Spondyloarthritis
- Spontaneous abortion
- Spontaneous bladder perforation
- Spontaneous breech delivery
- Spontaneous intestinal perforation
- Spontaneous labor and birth
- Spontaneous onset of labor
- Spontaneous perforation
- Spontaneous preterm birth
- Spontaneous rupture of membranes
- Spontaneous vertex delivery
- Sporadic hemiplegic migraine
- Square window sign
- Staphylococcus aureus infection
- Stat5b deficiency
- Status asthmaticus
- Status epilepticus
- Status migrainosus
- Steal syndrome
- Stenosis
- Step reflex
- Stereotypy
- Sternocleidomastoid injury related to birth
- Steroid 21-monooxygenase deficiency
- Steroidogenic acute regulatory protein deficiency
- Stertor
- Stevens johnson syndrome
- Stickler syndrome
- Stillbirth
- Stomatitis
- Strabismus
- Street number
- Streptococcal pharyngitis
- Stress dose steroid
- Stridor
- Stroller
- Strongyloidiasis
- Sturge-weber syndrome
- Stutter
- Stye
- Subacute bacterial endocarditis
- Subacute cutaneous lupus erythematosus
- Subacute granulomatous thyroiditis
- Subacute intervillous thrombus
- Subacute placental infarct
- Subacute sclerosing panencephalitis
- Subacute thyroiditis
- Subarachnoid hematoma
- Subarachnoid hemorrhage related to birth
- Subarachnoid hemorrhage
- Subcapsular hematoma
- Subchorial thrombus
- Subclavian vein stenosis
- Subclinical infection
- Subconjunctival hemorrhage
- Subcutaneous route of administration
- Subdiaphragmatic abscess
- Subdural hematoma
- Subdural hemorrhage related to birth
- Subdural hemorrhage
- Subependymal pseudocyst
- Subgaleal hematoma
- Subgaleal hemorrhage related to birth
- Subgaleal hemorrhage
- Submitting facility
- Subsequent relapse
- Substance
- Sucking reflex
- Sudden cardiac death
- Sudden infant death syndrome
- Sudden unexplained death in childhood
- Sudden unexplained infant death
- Suicidal ideation
- Suicide attempt
- Suicide
- Sunburn
- Superficial circumscribed morphea
- Superficial thrombophlebitis
- Superior vena cava occlusion
- Superior vena cava stenosis
- Superior vena cava syndrome
- Supplemental nursing system
- Suppurative arthritis
- Suppurative parotitis
- Supravalvular aortic stenosis
- Supravalvular pulmonary artery stenosis
- Supraventricular arrhythmia
- Supraventricular tachycardia
- Sur1-associated diabetes mellitus
- Surfactant protein a deficiency
- Surfactant protein abca3 deficiency
- Surfactant protein b deficiency
- Surfactant protein c deficiency
- Surfactant protein d deficiency
- Surfactant protein deficiency
- Surgical procedure
- Surgical site infection
- Surgical wound drain
- Surgical wound infection
- Surgically placed gastrostomy tube
- Susac syndrome
- Suspected necrotizing enterocolitis
- Swaddling
- Swan ganz catheter
- Sweat
- Sweating
- Swim diaper
- Symphysis pubis dysfunction
- Syncope
- Syndactyly
- Syndrome of apparent mineralocorticoid excess
- Syndrome of inappropriate antidiuretic hormone
- Syndrome
- Syngeneic
- Synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome
- Syphilis
- Systemic arterial hypertensive disorder
- Systemic corticosteroid
- Systemic disorder
- Systemic ebv-positive t-cell lymphoproliferative disease of childhood
- Systemic inflammatory response syndrome
- Systemic juvenile idiopathic arthritis
- Systemic juvenile rheumatoid arthritis (aq)
- Systemic lupus erythematosus disease activity index
- Systemic lupus erythematosus nephritis class I
- Systemic lupus erythematosus nephritis class ii
- Systemic lupus erythematosus nephritis class iii
- Systemic lupus erythematosus nephritis class iv g
- Systemic lupus erythematosus nephritis class iv s
- Systemic lupus erythematosus nephritis class iv
- Systemic lupus erythematosus nephritis class v
- Systemic lupus erythematosus nephritis class vi
- Systemic lupus erythematosus
- Systemic sclerosis without skin involvement
- Systemic sclerosis
- T acute lymphoblastic leukemia
- T-cell depletion
- T-tube
- Tabes dorsalis
- Tachyarrhythmia
- Tachycardia
- Tachypnea
- Tachysystole
- Tactile hallucination
- Taeniasis
- Takayasu arteritis
- Talipes
- Tall stature
- Targetoid lesion
- Tearfulness
- Teething
- Telephone number
- Telogen effluvium
- Temperature
- Temporal qualifier
- Tension-type headache
- Tentorial tear related to birth
- Teratoma
- Term birth
- Term infant
- Terminal hematuria
- Tertiary hyperparathyroidism
- Tertiary syphilis
- Testicular atrophy
- Testicular disorder
- Testicular failure
- Testicular germ cell tumor
- Testicular gonadoblastoma
- Testicular granulosa cell tumor
- Testicular hypotrophy
- Testicular involvement
- Testicular leydig cell tumor
- Testicular mixed germ cell-sex cord-stromal tumor
- Testicular regression
- Testicular sertoli cell tumor
- Testicular sex cord-stromal tumor
- Testicular torsion
- Testosterone biosynthesis deficiency
- Testosterone excess
- Tetanic contraction
- Tetanus and diphtheria toxoids adsorbed
- Tetanus toxoid vaccine
- Tetanus
- Tetany
- Tethered spinal cord syndrome
- Tetralogy of fallot - complete av canal defect
- Tetralogy of fallot
- Thalassemia
- Thalidomide embryopathy
- Thanatophoric dysplasia
- Therapeutic procedure
- Therapy related leukemia
- Therapy-related myeloid neoplasm
- Third degree burn
- Third degree perineal laceration
- Third trimester antepartum hemorrhage
- Thoracic meningocele
- Thoracic myelocele
- Thoracic myelomeningocele
- Threatened abortion
- Threatened preterm labor
- Threatened term labor
- Throat tightening
- Thrombocytopenia
- Thrombocytosis
- Thromboembolism
- Thrombophilia
- Thrombophlebitis
- Thrombosis
- Thrombotic microangiopathy
- Thrombotic thrombocytopenic purpura
- Thrombus
- Thumb hypoplasia
- Thymic damage
- Thyroglobulin deficiency
- Thyroglossal duct cyst
- Thyroid adenoma
- Thyroid agenesis
- Thyroid carcinoma
- Thyroid dysgenesis
- Thyroid dyshormonogenesis
- Thyroid hormone resistance
- Thyroid hypoplasia
- Thyroid nodule
- Thyroid peroxidase deficiency
- Thyroid sarcoma
- Thyroid stimulating hormone receptor gene mutation
- Thyroid stimulating hormone-producing adenoma
- Thyroid storm
- Thyroid tumor
- Thyroid-binding globulin deficiency
- Thyroid-binding globulin excess
- Thyroiditis
- Thyrotoxicosis
- Thyrotropin measurement
- Tibia fracture
- Tic
- Tick-borne relapsing fever
- Time of onset of labor
- Time
- Tinea infection
- Tinea versicolor
- Tinnitus
- Tip lesion glomerulopathy
- Tissue adhesion
- Tissue factor deficiency
- Tissue kallikrein deficiency
- Toddler stage
- Toddler
- Tonic neck reflex
- Tonsillitis
- Tonsillopharyngitis
- Tooth development disorder
- Tooth discoloration
- Tooth infection
- Tooth malformation
- Topical corticosteroid
- Torch antibody measurement
- Torch infection
- Torsades de pointes
- Total anomalous pulmonary venous return
- Total body length
- Total colonic aganglionosis
- Total intestinal aganglionosis
- Total thyroxine measurement
- Tourette syndrome
- Tourettism
- Townes-brocks syndrome
- Toxic epidermal necrolysis
- Toxic erythema of chemotherapy
- Toxic goiter
- Toxic methemoglobinemia with cyanosis
- Toxic shock syndrome
- Toxocariasis
- Toxoid vaccine
- Toxoplasmosis
- Tracheal agenesis
- Tracheal atresia
- Tracheal disorder
- Tracheal stenosis
- Tracheal web
- Tracheitis
- Tracheobronchitis
- Tracheoesophageal fistula
- Tracheomalacia
- Tracheostomy site
- Tracheostomy tube
- Tractional retinal detachment
- Transaminitis
- Transcription factor-associated monogenic diabetes
- Transferase deficiency galactosemia
- Transient abnormal myelopoiesis
- Transient erythroblastopenia of childhood
- Transient hyperinsulinism
- Transient hypogammaglobulinemia of infancy
- Transient hypothyroxinemia of prematurity
- Transient hypothyroxinemia
- Transient ischemic attacks
- Transient myocardial dysfunction of newborn
- Transient myocardial ischemia of newborn
- Transient neonatal diabetes mellitus
- Transient neonatal hyperparathyroidism
- Transient neonatal hypoparathyroidism
- Transient neonatal myasthenia gravis
- Transient neonatal pustular melanosis
- Transient primary hypothyroidism
- Transient tachypnea of the newborn
- Transient tic disorder
- Transitional cell carcinoma
- Transmission
- Transposition of great vessels
- Traumatic chylothorax
- Traumatic subcutaneous emphysema
- Travel cot
- Treacher collins syndrome
- Tremor
- Trial of labor after cesarean delivery
- Trichinosis
- Trichuriasis
- Tricuspid valve atresia
- Tricuspid valve regurgitation
- Tricuspid valve stenosis
- Trigeminal autonomic cephalalgia
- Trigonitis
- Trimmed placental weight
- Triosephosphate isomerase deficiency
- Triple a syndrome
- Triplet pregnancy
- Triploidy syndrome
- Trisomy 18
- Trisomy 21
- Tsh resistance
- Tubal pregnancy
- Tuberculin skin test
- Tuberculosis infection
- Tuberculosis
- Tuberous sclerosis
- Tubulointerstitial disease
- Tubulointerstitial nephritis and uveitis
- Tubulointerstitial nephritis
- Tularemia
- Tumor lysis syndrome
- Tumor necrosis factor receptor 1-associated periodic syndrome
- Turner syndrome
- Twin pregnancy
- Twin reversed arterial perfusion sequence malformation
- Twin-twin transfusion syndrome
- Txnrd2-associated fgd
- Ty21a typhoid vaccine
- Tympanostomy tube
- Type 1 diabetes mellitus
- Type 1 thanatophoric dysplasia
- Type 2 diabetes mellitus
- Type 2 thanatophoric dysplasia
- Type I acrocephalosyndactyly
- Type I immediate hypersensitivity reaction
- Type I pleuropulmonary blastoma
- Type I renal tubular acidosis
- Type I total anomalous pulmonary venous return
- Type ii acrocephalopolysyndactyly
- Type ii hypersensitivity reaction
- Type ii pleuropulmonary blastoma
- Type ii total anomalous pulmonary venous return
- Type iii hypersensitivity reaction
- Type iii pleuropulmonary blastoma
- Type iii total anomalous pulmonary venous return
- Type iv hypersensitivity reaction
- Type iv total anomalous pulmonary venous return
- Type v acrocephalosyndactyly
- Typhlitis
- Typhoid fever
- Tyrosinemia type I
- USMLE
- Ulcer
- Ulcerative colitis flare
- Ulcerative colitis
- Ultrasonography
- Umbilical cord compression
- Umbilical cord diameter
- Umbilical cord discoloration
- Umbilical cord length
- Umbilical cord occlusion
- Umbilical cord prolapse
- Umbilical cord true knot
- Umbilical granuloma
- Umbilical hernia
- Umbilical vasculitis
- Unconjugated hyperbilirubinemia
- Uncuffed dialysis catheter
- Undifferentiated connective tissue disease
- Undifferentiated juvenile idiopathic arthritis
- Unifocal langerhans cell histiocytosis
- Uniform color of placental parenchyma
- Unilateral anophthalmos
- Unilateral microphthalmos
- Unilateral optic nerve hypoplasia
- Unilateral renal agenesis
- Uninodular goiter
- Unit of measure
- Unit per gram
- Unknown group b streptococcus risk status
- Unresponsive to stimuli
- Untrimmed placental weight
- Upper respiratory infection
- Urachal cyst
- Urachal diverticulum
- Urachal remnant
- Urea cycle metabolism disorder
- Uremic pericarditis
- Ureter disorder
- Ureter fissus
- Ureteral anastomotic leak
- Ureteral compression
- Ureteral kinking
- Ureteral obstruction
- Ureteral perforation
- Ureteral stenosis
- Ureteral stricture
- Ureteritis
- Ureterocele
- Ureterovesical obstruction
- Urethral prolapse
- Urethral stricture
- Urethritis
- Urethrotrigonitis
- Uric acid nephrolithiasis
- Uric acid urolithiasis
- Urinary casts
- Urinary frequency
- Urinary hesitancy
- Urinary incontinence
- Urinary leak
- Urinary retention
- Urinary straining
- Urinary system disorder
- Urinary system finding
- Urinary tract infection
- Urinary tract obstruction
- Urinary tract stenosis
- Urinary urgency
- Urine output decreased
- Urolithiasis
- Urostomy site
- Urticaria
- Us state
- Uterine agenesis
- Uterine dehiscence
- Uteroplacental vessel fibrinoid necrosis with or without atherosis
- Uteroplacental vessel thrombus
- Utp-hexose-1-phosphate uridylyltransferase deficiency
- Uveal prolapse
- Uveitis
- Uvulitis
- Vaccine-associated paralytic poliomyelitis
- Vaccine
- Vacterl association
- Vacuum assisted vaginal delivery
- Vacuum extraction chignon
- Vaginal assisted delivery
- Vaginal birth after cesarean delivery
- Vaginal delivery
- Vaginal discharge
- Vaginal fistula
- Vaginitis
- Valentini scleroderma disease activity index
- Valvular heart disorder
- Van der woude syndrome
- Vanishing twin syndrome
- Variable fetal heart rate deceleration
- Variant creutzfeldt-jakob disease
- Varicella vaccine
- Varicella zoster infection
- Varicella zoster virus immunization
- Varicella zoster virus
- Varicella
- Varicose vein of lower extremities
- Vasa previa
- Vascular calcification
- Vascular disorder
- Vascular malformation
- Vascular ring
- Vascular stenosis
- Vasculitic ulcer
- Vasculitis
- Vaso-occlusive crisis
- Vasovagal reaction
- Vector transmission
- Vector
- Vehicle transmission
- Vein of galen malformation
- Velamentous cord insertion
- Velamentous vessel
- Venous catheter
- Venous embolism
- Venous stroke
- Venous thromboembolism
- Venous thrombosis related to vascular access complication
- Venous thrombosis
- Ventral hernia
- Ventricular arrhythmia
- Ventricular dysfunction
- Ventricular fibrillation
- Ventricular septal defect
- Ventricular tachycardia
- Ventriculostomy drain
- Vernier caliper
- Verruca plantaris
- Verruca vulgaris
- Vertex presentation
- Vertigo
- Very long-chain acyl-coa dehydrogenase deficiency
- Very low birth weight
- Very preterm infant
- Vesicle
- Vesicoureteral reflux
- Vi capsular polysaccharide typhoid vaccine
- Vibroacoustic stimulation
- Violent behavior
- Viral conjunctivitis
- Viral gastroenteritis
- Viral hemorrhagic fever
- Viral hepatitis
- Viral infection
- Viral meningitis
- Viral myocarditis
- Viral pericarditis
- Virilization in girls
- Virilization
- Virus
- Vision disorder
- Visual cortex disorder
- Visual field defect
- Visual hallucination
- Vital sign measurement
- Vitamin b12 deficiency
- Vitamin b6 deficiency
- Vitamin d 1 alpha-hydroxylase deficiency
- Vitamin d 25-hydroxylase deficiency
- Vitamin d deficiency
- Vitamin d receptor deficiency rickets
- Vitamin d receptor deficiency
- Vitamin d receptor signaling defect rickets
- Vitamin deficiency disorder
- Vitamin k deficiency
- Vitamin k
- Vitiligo
- Vitreous hemorrhage
- Vocal cord paralysis
- Voiding disorders
- Vomiting
- Von hippel-lindau syndrome
- Von willebrand disease, type 1
- Von willebrand disease, type 2a
- Von willebrand disease, type 2b
- Von willebrand disease, type 2m
- Von willebrand disease, type 2n
- Von willebrand disease, type 3
- Von willebrand disease
- Vulvovaginal candidiasis
- Vulvovaginitis
- Waardenburg syndrome
- Wagr syndrome
- Wagro syndrome
- Walker-warburg syndrome
- Walking pneumonia
- Wandering atrial pacemaker
- Wart
- Waterhouse-friderichsen syndrome
- Watering eyes
- Weak breathing
- Weakness
- Weaning
- Weaver syndrome
- Weight gain
- Weight loss
- Wellness
- Werdnig-hoffmann disease
- West syndrome
- Wet nurse
- Wheezing
- Whipple disease
- White matter injury
- Whooping cough
- WikiMD
- Williams syndrome
- Wilms tumor 1 gene syndromes
- Wilms tumor
- Wiskott-aldrich syndrome
- Wnt4 deficiency
- Wolcott-rallison syndrome
- Wolff-chaikoff
- Wolff-parkinson-white syndrome
- Wolfram syndrome
- Wound botulism
- Wound discharge
- Wound disruption
- Wound infection
- X-linked adrenal hypoplasia congenita
- X-linked dominant hypophosphatemic rickets
- X-linked hypoparathyroidism
- X-linked hypophosphatemic rickets
- X-linked recessive hypophosphatemic rickets
- Xanthogranulomatous pyelonephritis
- Xerostomia
- Yawning
- Yeast
- Yellow fever vaccine
- Yellow fever
- Yersiniosis
- Yes
- Zellweger syndrome
- Zika
- Zoonotic infection
- Zoster
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