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| Line 1: |
Line 1: |
| * [[AIDS dementia complex]]
| | {{div col|colwidth=15em}} |
| * [[ATR-X]]
| | |
| * [[Aarskog–Ose–Pande syndrome]]
| |
| * [[Abdominal defects]]
| |
| * [[Abdominal musculature absent microphthalmia joint laxity]] | | * [[Abdominal musculature absent microphthalmia joint laxity]] |
| * [[Acanthocytosis chorea]]
| |
| * [[Achalasia alacrimia syndrome]]
| |
| * [[Achalasia, familial esophageal]]
| |
| * [[Acitretine antenatal infection]]
| |
| * [[Acoustic schwannomas]]
| |
| * [[Acquired central hypoventilation syndrome]]
| |
| * [[Acyl-CoA dehydrogenase, medium chain, deficiency of]]
| |
| * [[Acyl-CoA dehydrogenase, short chain, deficiency of]]
| |
| * [[Acyl-CoA dehydrogenase, very long chain, deficiency of]] | | * [[Acyl-CoA dehydrogenase, very long chain, deficiency of]] |
| * [[Adrenal disorder]]
| |
| * [[Adrenal gland hyperfunction]]
| |
| * [[Adrenal hypertension]]
| |
| * [[Adult syndrome]]
| |
| * [[Agnosia, primary visual]]
| |
| * [[Ahumada-Del Castillo syndrome]]
| |
| * [[Alagille–Watson syndrome (AWS)]]
| |
| * [[Albers–Schonberg disease]]
| |
| * [[Alopecia contractures dwarfism mental retardation]]
| |
| * [[Alport syndrome, dominant type]]
| |
| * [[Alport syndrome, recessive type]]
| |
| * [[Amaurosis congenita of Leber]]
| |
| * [[Amaurosis congenita of Leber, type 1]]
| |
| * [[Amaurosis congenita of Leber, type 2]]
| |
| * [[Amelia cleft lip palate hydrocephalus iris coloboma]]
| |
| * [[Amnesic shellfish poisoning]]
| |
| * [[Anemia, Diamond–Blackfan]]
| |
| * [[Anemia, hypoplastic, congenital]]
| |
| * [[Anemia, pernicious]]
| |
| * [[Aneurysm, intracranial berry]]
| |
| * [[Aniridia absent patella]]
| |
| * [[Aniridia ataxia renal agenesis psychomotor retardation]]
| |
| * [[Aniridia cerebellar ataxia mental deficiency]]
| |
| * [[Aniridia type 2]]
| |
| * [[Aniridia, sporadic]]
| |
| * [[Anophthalmos, clinical]]
| |
| * [[Anorectal atresia]]
| |
| * [[Anorectal malformation]]
| |
| * [[Antithrombin deficiency, congenital]]
| |
| * [[Aortic window]]
| |
| * [[Apiphobia]]
| |
| * [[Apraxia, Ideomotor]]
| |
| * [[Arc syndrome]]
| |
| * [[Arrythmogenic right ventricular dysplasia, familial]]
| |
| * [[Arthritis, juvenile]]
| |
| * [[Arthrogryposis ectodermal dysplasia other anomalies]]
| |
| * [[Arthrogryposis multiplex congenita, distal type 1]]
| |
| * [[Arthrogryposis multiplex congenita, distal type 2]]
| |
| * [[Arthrogryposis multiplex congenita, distal, x-linked]]
| |
| * [[Autoimmune peripheral neuropathy]]
| |
| * [[Avian Flu]]
| |
| * [[B-cell lymphomas]]
| |
| * [[BANF acoustic neurinoma]]
| |
| * [[Balo disease]]
| |
| * [[Balo's concentric sclerosis]]
| |
| * [[Bannayan–Zonana syndrome]]
| |
| * [[Bartsocas–Papas syndrome]]
| |
| * [[Basal ganglia diseases]]
| |
| * [[Bathophobia]]
| |
| * [[Batrachophobia]]
| |
| * [[Becker disease]]
| |
| * [[Beemer–Langer syndrome]]
| |
| * [[Berardinelli–Seip congenital lipodystrophy]]
| |
| * [[Berlin breakage syndrome]]
| |
| * [[Bickel Fanconi glycogenosis]]
| |
| * [[Bilateral renal agenesis dominant type]]
| |
| * [[Biliary atresia, extrahepatic]]
| |
| * [[Blepharo naso facial syndrome Van maldergem type]]
| |
| * [[Blepharophimosis, ptosis, epicanthus inversus]]
| |
| * [[Bone fragility craniosynostosis proptosis hydrocephalus]]
| |
| * [[Bone tumor (generic term)]]
| |
| * [[Bonnevie–Ullrich–Turner syndrome]]
| |
| * [[Bourneville's disease]]
| |
| * [[Brachman-de Lange syndrome]]
| |
| * [[Brachydactyly Smorgasbord type]]
| |
| * [[Brachydactyly clinodactyly]]
| |
| * [[Brachydactyly type A5 nail dysplasia]]
| |
| * [[Brachymesophalangy 2 and 5]]
| |
| * [[Bronchitis, Chronic]]
| |
| * [[CATCH 22 syndrome]]
| |
| * [[CDG syndrome]]
| |
| * [[CDG syndrome type 1A]]
| |
| * [[CHILD syndrome ichthyosis]]
| |
| * [[Cacchi–Ricci disease]]
| |
| * [[Camfak syndrome]]
| |
| * [[Cannabis withdrawal]]
| |
| * [[Carbohydrate deficient glycoprotein syndrome]]
| |
| * [[Carcinophobia]]
| |
| * [[Cardiomyopathy, familial hypertrophic]]
| |
| * [[Caregiver syndrome]]
| |
| * [[Cayler syndrome]]
| |
| * [[Centronuclear myopathy (including myotubular myopathy)]]
| |
| * [[Centronuclear myopathy (including myotubular myopathy)]]
| |
| * [[Centronuclear myopathy (including myotubular myopathy)]]
| |
| * [[Cerebral amyloid angiopathy, familial]]
| |
| * [[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy]]
| |
| * [[Cerebral ventricle neoplasms]]
| |
| * [[Cerebro facio articular syndrome]]
| |
| * [[Ceroid lipofuscinois, neuronal 1, infantile]]
| |
| * [[Ceroid lipofuscinois, neuronal 2, late infantile]]
| |
| * [[Ceroid lipofuscinois, neuronal 3, juvenile]]
| |
| * [[Ceroid lipofuscinois, neuronal 4, adult type]]
| |
| * [[Ceroid lipofuscinois, neuronal 5, late infantile]]
| |
| * [[Ceroid lipofuscinois, neuronal 6, late infantile]]
| |
| * [[Chanarin–Dorfman syndrome ichthyosis]]
| |
| * [[Chang–Davidson–Carlson syndrome]]
| |
| * [[Chavany–Brunhes syndrome]]
| |
| * [[Chediak–Higashi syndrome]]
| |
| * [[Chen-Kung Ho–Kaufman–Mcalister syndrome]]
| |
| * [[Chiari type 1 malformation]]
| |
| * [[Childhood pustular psoriasis]]
| |
| * [[Cholestasis, progressive familial intrahepatic]]
| |
| * [[Cholestasis, progressive familial intrahepatic 1]]
| |
| * [[Cholestasis, progressive familial intrahepatic 2]]
| |
| * [[Cholestasis, progressive familial intrahepatic 3]]
| |
| * [[Chondrocalcinosis familial articular]]
| |
| * [[Chondrodysplasia punctata 1, x-linked recessive]]
| |
| * [[Chondrodysplasia punctata, brachytelephalangic]]
| |
| * [[Chondromalacia]]
| |
| * [[Chorea minor]]
| |
| * [[Choreoathetosis familial paroxysmal]]
| |
| * [[Choroiditis, serpiginous]]
| |
| * [[Chromophobe renal carcinoma]]
| |
| * [[Chromosome 1, 1p36 deletion syndrome]]
| |
| * [[Chromosome 15q, partial deletion]]
| |
| * [[Chromosome 18, trisomy]]
| |
| * [[Chromosome 2, monosomy 2q37]]
| |
| * [[Chromosome 20 ring]]
| |
| * [[Chronic, infantile, neurological, cutaneous, articular syndrome]]
| |
| * [[Churg–Strauss syndrome]]
| |
| * [[Cleft lip with or without cleft palate]]
| |
| * [[Cockayne syndrome type 1]]
| |
| * [[Cockayne syndrome type 2]]
| |
| * [[Cogan–Reese syndrome]]
| |
| * [[Cold agglutination syndrome]]
| |
| * [[Cold antibody hemolytic anemia (disambiguation)]]
| |
| * [[Cole carpenter syndrome]]
| |
| * [[Collagen disorder]]
| |
| * [[Colon cancer, familial nonpolyposis]]
| |
| * [[Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency]]
| |
| * [[Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency]]
| |
| * [[Congenital antithrombin III deficiency]]
| |
| * [[Congenital constricting band]]
| |
| * [[Congenital cystic adenomatoid malformation]]
| |
| * [[Congenital ichtyosiform erythroderma]]
| |
| * [[Congenital megaloureter]]
| |
| * [[Congenital short bowel]]
| |
| * [[Congenital spherocytic anemia]]
| |
| * [[Congenital spherocytic hemolytic anemia]]
| |
| * [[Constrictive bronchiolitis]]
| |
| * [[Costal chondritis]]
| |
| * [[Cote–Adamopoulos–Pantelakis syndrome]]
| |
| * [[Cousin–Walbraum–Cegarra syndrome]]
| |
| * [[Covesdem syndrome]]
| |
| * [[Cowchock–Wapner–Kurtz syndrome]]
| |
| * [[Creatine deficiency]]
| |
| * [[Creeping disease]]
| |
| * [[Crystal deposit disease]]
| |
| * [[Cutaneous vascularitis]]
| |
| * [[Cutis laxa corneal clouding mental retardation]]
| |
| * [[Cutis laxa with joint laxity and retarded development]]
| |
| * [[Cutis laxa, dominant type]]
| |
| * [[Cutis laxa, recessive]]
| |
| * [[Cutis laxa, recessive type 1]]
| |
| * [[Cutis laxa, recessive type 2]]
| |
| * [[Cystin transport, protein defect of]]
| |
| * [[Cytochrome C oxidase deficiency]]
| |
| * [[Dandy–Walker syndrome]]
| |
| * [[Death anxiety]]
| |
| * [[Deciduous skin]]
| |
| * [[Decompensated phoria]]
| |
| * [[Dentin dysplasia, radicular]]
| |
| * [[Der Kaloustian–Jarudi–Khoury syndrome]]
| |
| * [[Dermatoosteolysis, Kirghizian type]]
| |
| * [[Dermatophytids]]
| |
| * [[Desbuquois Syndrome]]
| |
| * [[Diabetes insipidus, nephrogenic type 1]]
| |
| * [[Diabetes insipidus, nephrogenic type 2]]
| |
| * [[Diabetes insipidus, nephrogenic type 3]]
| |
| * [[Diabetes insipidus, nephrogenic, dominant type]]
| |
| * [[Diabetes insipidus, nephrogenic, recessive type]]
| |
| * [[Diarrheal shellfish poisoning]]
| |
| * [[Disaccharide intolerance iii]]
| |
| * [[Disinhibited attachment disorder]]
| |
| * [[Donnai Barrow syndrome]]
| |
| * [[Double cortex]]
| |
| * [[Dust-induced lung disease]]
| |
| * [[Dysencephalia splachnocystica or Meckel–Gruber]]
| |
| * [[Dyserythropoietic anemia, congenital]]
| |
| * [[Dyserythropoietic anemia, congenital type 1]]
| |
| * [[Dyserythropoietic anemia, congenital type 2]]
| |
| * [[Dyserythropoietic anemia, congenital type 3]]
| |
| * [[Dysphonia, chronic spasmodic]]
| |
| * [[Eec syndrome without cleft lip palate]]
| |
| * [[Eem syndrome]]
| |
| * [[Egg hypersensitivity]]
| |
| * [[Ekbom syndrome (disambiguation)]]
| |
| * [[Encephalomyelitis, myalgic]]
| |
| * [[Encephalotrigeminal Angiomatosis]]
| |
| * [[Enchondromatosis (benign)]]
| |
| * [[Enetophobia]]
| |
| * [[Envenomization by bothrops lanceolatus]]
| |
| * [[Envenomization by the Martinique lancehead viper]] | | * [[Envenomization by the Martinique lancehead viper]] |
| * [[Epimerase deficiency]]
| |
| * [[Erb–Duchenne palsy]]
| |
| * [[Erythroblastopenia (disambiguation)]]
| |
| * [[Erythrokeratodermia ataxia]]
| |
| * [[Erythrokeratodermia variabilis, Mendes da Costa type]]
| |
| * [[Erythrokeratolysis hiemalis ichthyosis]]
| |
| * [[Essential iris atrophy]]
| |
| * [[Essential mixed cryoglobulinemia]]
| |
| * [[Ethylmalonic aciduria]]
| |
| * [[Ethylmalonic adipic aciduria]]
| |
| * [[Eunuchoidism familial]]
| |
| * [[Exercise induced anaphylaxis]]
| |
| * [[Exner syndrome]]
| |
| * [[Extrapyramidal disorder]]
| |
| * [[Eye movement (sensory)#Disorders]]
| |
| * [[Faces syndrome]]
| |
| * [[Facial dysmorphism shawl scrotum joint laxity syndrome]]
| |
| * [[Facial paralysis]]
| |
| * [[Familial Treacher–Collins syndrome]]
| |
| * [[Familial cold autoinflamatory syndrome (FCAS)]]
| |
| * [[Familial hyperchylomicronemia]]
| |
| * [[Familial hyperlipoproteinemia type III]]
| |
| * [[Familial hyperlipoproteinemia type IV]] | | * [[Familial hyperlipoproteinemia type IV]] |
| * [[Familial hypersensitivity pneumonitis]]
| |
| * [[Familial intestinal polyatresia syndrome]]
| |
| * [[Familial nasal acilia]]
| |
| * [[Fanconi anemia type 1]]
| |
| * [[Fanconi anemia type 2]]
| |
| * [[Fanconi anemia type 3]]
| |
| * [[Fanconi syndrome, renal, with nephrocalcinosis and renal stones]]
| |
| * [[Fazio–Londe syndrome]]
| |
| * [[Ferrocalcinosis cerebro vascular]]
| |
| * [[Fetal methyl mercury syndrome]]
| |
| * [[Fibrolipomatosis]]
| |
| * [[Flavimonas oryzihabitans]]
| |
| * [[Fluorosis (disambiguation)]]
| |
| * [[Follicular ichthyosis]]
| |
| * [[Forbes–Albright syndrome]]
| |
| * [[Froelich's syndrome]]
| |
| * [[Frontonasal dysplasia Klippel–Feil syndrome]]
| |
| * [[Fructose-1-phosphate aldolase deficiency, heredita]]
| |
| * [[Fructosemia, hereditary]]
| |
| * [[Fukuyama-type muscular dystrophy]]
| |
| * [[Fumaric aciduria]]
| |
| * [[Galactosamine-6-sulfatase deficiency]]
| |
| * [[Gangliosidosis (Type2)(GM2)]]
| |
| * [[Gangliosidosis type1]]
| |
| * [[Gas/bloat syndrome]]
| |
| * [[Gastrointestinal neoplasm]]
| |
| * [[Gemss syndrome]]
| |
| * [[Genetic diseases, inborn]]
| |
| * [[Genital retraction syndrome]]
| |
| * [[Genuphobia]]
| |
| * [[Genée-Wiedemann syndrome]]
| |
| * [[German syndrome]]
| |
| * [[Gianotti-Crosti syndrome]]
| |
| * [[Giant congenital nevi]]
| |
| * [[Glaucoma, primary infantile type 3B]]
| |
| * [[Gloomy face syndrome]]
| |
| * [[Glucocorticoid deficiency, familial]]
| |
| * [[Glutaricaciduria I]]
| |
| * [[Glutaricaciduria II]]
| |
| * [[Glycogen storage disease type 1C]]
| |
| * [[Glycogen storage disease type 6, due to phosphorylation]]
| |
| * [[Glycogen storage disease type 9]]
| |
| * [[Glycogen storage disease type VIII]]
| |
| * [[Glycogenosis type III]]
| |
| * [[Glycogenosis type V]]
| |
| * [[Glycogenosis type VI]]
| |
| * [[Glycogenosis type VIII]]
| |
| * [[Glycogenosis, type 0]]
| |
| * [[Gomez and López-Hernández syndrome]]
| |
| * [[Gonadal dysgenesis, XY female type]]
| |
| * [[Gordon Syndrome]]
| |
| * [[Gottron's syndrome]]
| |
| * [[Granulomatosis, lymphomatoid]]
| |
| * [[Greenberg dysplasia]]
| |
| * [[Gyrate atrophy of the choroid and retina]]
| |
| * [[Gyrate atrophy of the retina]]
| |
| * [[HIV dementia]] | | * [[HIV dementia]] |
| * [[HSV-2 infection]] | | * [[HSV-2 infection]] |
| * [[Hageman factor deficiency]]
| |
| * [[Hamartoma sebaceus of Jadassohn]] | | * [[Hamartoma sebaceus of Jadassohn]] |
| * [[Hand wringing Rett syndrome]]
| |
| * [[Hand–foot–uterus syndrome]]
| |
| * [[Harlequin type ichthyosis]] | | * [[Harlequin type ichthyosis]] |
| * [[Harpaxophobia]] | | * [[Harpaxophobia]] |
| * [[Hashimoto struma]]
| |
| * [[Headache, cluster]]
| |
| * [[Heart aneurysm]]
| |
| * [[Heart hypertrophy, hereditary]]
| |
| * [[Heart situs anomaly]]
| |
| * [[Heart tumor of the adult]]
| |
| * [[Heart tumor of the child]]
| |
| * [[Hemiplegic migraine, familial]]
| |
| * [[Hemochromatosis type 1]]
| |
| * [[Hemophobia]] | | * [[Hemophobia]] |
| * [[Hepadnovirus D]] | | * [[Hepadnovirus D]] |
| * [[Hepatic venoocclusive disease]]
| |
| * [[Hereditary breast—ovarian cancer syndrome]] | | * [[Hereditary breast—ovarian cancer syndrome]] |
| * [[Hereditary carnitine deficiency]]
| |
| * [[Hereditary carnitine deficiency myopathy]]
| |
| * [[Hereditary ceroid lipofuscinosis]]
| |
| * [[Hereditary hearing disorder]] | | * [[Hereditary hearing disorder]] |
| * [[Hereditary hearing loss]] | | * [[Hereditary hearing loss]] |
| * [[Hereditary hyperuricemia]]
| |
| * [[Hereditary methemoglobinemia, recessive]]
| |
| * [[Hereditary non-spherocytic hemolytic anemia]]
| |
| * [[Hereditary peripheral nervous disorder]]
| |
| * [[Hereditary primary Fanconi disease]]
| |
| * [[Hereditary sensory and autonomic neuropathy 3]]
| |
| * [[Hereditary sensory and autonomic neuropathy 4]]
| |
| * [[Herpes simplex disease]]
| |
| * [[Herpes viridae disease]]
| |
| * [[Herpetic keratitis]]
| |
| * [[Hers' disease]]
| |
| * [[Heterophobia]] | | * [[Heterophobia]] |
| * [[Heterotaxia (generic term)]]
| |
| * [[High scapula]]
| |
| * [[Hip dysplasia (human)]] | | * [[Hip dysplasia (human)]] |
| * [[Hip luxation]]
| |
| * [[Histadelia]] | | * [[Histadelia]] |
| * [[Histapenia]] | | * [[Histapenia]] |
| * [[Histiocytosis, Non-Langerhans-Cell]]
| |
| * [[Hm syndrome]]
| |
| * [[Holmes–Gang syndrome]]
| |
| * [[Homocystinuria due to cystathionine beta-synthase]]
| |
| * [[Horn–Kolb syndrome]]
| |
| * [[Horton disease, juvenile]]
| |
| * [[Hutchinson–Gilford–Progeria syndrome]]
| |
| * [[Hydrocephalus - Arnold Chiari - allied disorders]] | | * [[Hydrocephalus - Arnold Chiari - allied disorders]] |
| * [[Hyper IgE]] | | * [[Hyper IgE]] |
| * [[Hyper-reninism]] | | * [[Hyper-reninism]] |
| * [[Hyperaldosteronism familial type 2]]
| |
| * [[Hyperimmunoglobinemia D with recurrent fever]]
| |
| * [[Hyperimmunoglobinemia D with recurrent fever]]
| |
| * [[Hyperimmunoglobulinemia E]] | | * [[Hyperimmunoglobulinemia E]] |
| * [[Hyperinsulinism in children, congenital]]
| |
| * [[Hyperinsulinism, focal]]
| |
| * [[Hyperornithinemia, hyperammonemia, homocitrullinuria syndrome]]
| |
| * [[Hyperostosis Corticalis Generalisata]]
| |
| * [[Hyperoxaluria type 1]]
| |
| * [[Hypertrichosis lanuginosa congenita]]
| |
| * [[Hypertriglycidemia]] | | * [[Hypertriglycidemia]] |
| * [[Hypobetalipoprotéinemia, familial]]
| |
| * [[Hypodontia of incisors and premolars]]
| |
| * [[Hypokalemic periodic paralysis type 1]]
| |
| * [[Hypomentia]] | | * [[Hypomentia]] |
| * [[Hypopituitary dwarfism]] | | * [[Hypopituitary dwarfism]] |
| * [[Ichthyophobia]] | | * [[Ichthyophobia]] |
| * [[Ichthyosis deafness mental retardation skeletal anomaly]]
| |
| * [[Ichthyosis, Netherton syndrome]]
| |
| * [[Idiopathic hypercalcinuria]]
| |
| * [[Iduronate 2-sulfatase deficiency]]
| |
| * [[Inborn metabolic disorder]] | | * [[Inborn metabolic disorder]] |
| * [[Incisors fused]]
| |
| * [[Indomethacin antenatal infection]]
| |
| * [[Infantile sialic acid storage disorder]]
| |
| * [[Intestinal pseudoobstruction chronic idiopathic]]
| |
| * [[Intracranial arteriovenous malformations]]
| |
| * [[Intrauterine infections]] | | * [[Intrauterine infections]] |
| * [[Iodine antenatal infection]] | | * [[Iodine antenatal infection]] |
| * [[Iophobia]] | | * [[Iophobia]] |
| * [[Isosporosiasis]] | | * [[Isosporosiasis]] |
| * [[Isotretinoin embryopathy]]
| |
| * [[Jankovic–Rivera syndrome]]
| |
| * [[Jarcho–Levin syndrome]]
| |
| * [[Juberg–Marsidi syndrome]]
| |
| * [[Karsch–Neugebauer syndrome]]
| |
| * [[Ki-1cell lymphoma]]
| |
| * [[King–Denborough syndrome]]
| |
| * [[Klippel–Feil syndrome dominant type]]
| |
| * [[Klippel–Feil syndrome recessive type]]
| |
| * [[Kobberling–Dunnigan syndrome]]
| |
| * [[Kounis syndrome]]
| |
| * [[Krause–Kivlin syndrome]]
| |
| * [[L-transposition and ccTGA]] | | * [[L-transposition and ccTGA]] |
| * [[LGCR]] | | * [[LGCR]] |
| * [[Lambert–Eaton syndrome]]
| |
| * [[Lamellar recessive ichthyosis]]
| |
| * [[Landouzy–Dejerine muscular dystrophy]]
| |
| * [[Langdon Down]] | | * [[Langdon Down]] |
| * [[Large B-cell diffuse lymphoma]]
| |
| * [[Lattice corneal dystrophy type 2]] | | * [[Lattice corneal dystrophy type 2]] |
| * [[Launois–Bensaude adenolipomatosis]] | | * [[Launois–Bensaude adenolipomatosis]] |
| * [[Leber's disease]]
| |
| * [[Legg–Calvé–Perthes syndrome]]
| |
| * [[Lenz–Majewski hyperostotic dwarfism]]
| |
| * [[Levine–Crichley syndrome]]
| |
| * [[Light chain disease]]
| |
| * [[Lissencephaly, isolated]]
| |
| * [[Lutz–Lewandowsky epidermodysplasia verruciformis]] | | * [[Lutz–Lewandowsky epidermodysplasia verruciformis]] |
| * [[LyP (lymphomatoid papulosis)]]
| |
| * [[Lygophobia]] | | * [[Lygophobia]] |
| * [[Lymphedema hereditary type 1]]
| |
| * [[Lymphedema hereditary type 2]]
| |
| * [[Lymphoma, AIDS-related]]
| |
| * [[Lymphoma, small cleaved-cell, diffuse]]
| |
| * [[Lymphoma, small cleaved-cell, follicular]]
| |
| * [[Lymphomatoid Papulosis (LyP)]]
| |
| * [[MPS III-A]] | | * [[MPS III-A]] |
| * [[MPS III-B]] | | * [[MPS III-B]] |
| Line 411: |
Line 44: |
| * [[MPS III-D]] | | * [[MPS III-D]] |
| * [[MRKH Syndrome]] | | * [[MRKH Syndrome]] |
| * [[MTHFR deficiency]]
| |
| * [[Macrocephaly cutis marmorata telangiectatica]]
| |
| * [[Macroglossia exomphalos gigantism]] | | * [[Macroglossia exomphalos gigantism]] |
| * [[Macrothrombocytopenia with leukocyte inclusions]]
| |
| * [[Macular dystrophy, vitelliform]]
| |
| * [[Male pseudohermaphroditism due to 17-beta-hydroxysteroid dehydrogenase deficiency]]
| |
| * [[Marburg fever]]
| |
| * [[Marfan Syndrome type II]]
| |
| * [[Marfanoid hypermobility]]
| |
| * [[Mayer–Rokitanski–Kuster syndrome]]
| |
| * [[McArdle disease]]
| |
| * [[Medium-chain Acyl-CoA dehydrogenase deficiency]] | | * [[Medium-chain Acyl-CoA dehydrogenase deficiency]] |
| * [[Medullary cystic disease]]
| |
| * [[Mega-epiphyseal dwarfism]]
| |
| * [[Mental retardation, X linked, Marfanoid habitus]]
| |
| * [[Metastatic Insulinoma]] | | * [[Metastatic Insulinoma]] |
| * [[Methimazole antenatal infection]]
| |
| * [[Methyl mercury antenatal infection]]
| |
| * [[Meyenburg–Altherr–Uehlinger syndrome]]
| |
| * [[Microphthalmia, Lentz type]]
| |
| * [[Miculicz syndrome]]
| |
| * [[Mitochondrial myopathy-encephalopathy-lactic acidosis]]
| |
| * [[Mitral valve prolapse, familial, X linked]]
| |
| * [[Moeschler–Clarren syndrome]]
| |
| * [[Mohr syndrome]]
| |
| * [[Monge's disease]]
| |
| * [[Morphea, generalized]]
| |
| * [[Morse–Rawnsley–Sargent syndrome]]
| |
| * [[Motor neuropathy]]
| |
| * [[Motor sensory neuropathy type 1 aplasia cutis congenita]] | | * [[Motor sensory neuropathy type 1 aplasia cutis congenita]] |
| * [[Mount–Reback syndrome]]
| |
| * [[Mucolipidosis type 3]] | | * [[Mucolipidosis type 3]] |
| * [[Mucopolysaccharidosis type I Hurler syndrome]]
| |
| * [[Mucopolysaccharidosis type I Hurler/Scheie syndrome]]
| |
| * [[Mucopolysaccharidosis type I Scheie syndrome]]
| |
| * [[Mucopolysaccharidosis type II Hunter syndrome- mild form]]
| |
| * [[Mucopolysaccharidosis type II Hunter syndrome- severe form]]
| |
| * [[Mucopolysaccharidosis type IV-A Morquio syndrome]]
| |
| * [[Mucopolysaccharidosis type VI Maroteaux-Lamy - severe, intermediate]] | | * [[Mucopolysaccharidosis type VI Maroteaux-Lamy - severe, intermediate]] |
| * [[Mucopolysaccharidosis type VII Sly syndrome]]
| |
| * [[Multifocal ventricular premature beats]]
| |
| * [[Multiple organ failure]] | | * [[Multiple organ failure]] |
| * [[Muscle-eye-brain syndrome]]
| |
| * [[Muscular dystrophy, Duchenne and Becker type]]
| |
| * [[Muscular dystrophy, facioscapulohumeral]]
| |
| * [[Myalgia eosinophilia associated with tryptophan]]
| |
| * [[Myasthenia, familial]]
| |
| * [[Mycobacterium avium complex infection]]
| |
| * [[Mycosis fungoides, familial]]
| |
| * [[Mycositis fungoides]]
| |
| * [[Myelofibrosis, idiopathic]]
| |
| * [[Myoadenylate deaminase deficiency]]
| |
| * [[Myocardium disorder]]
| |
| * [[Myoclonic epilepsy with ragged red fibres]]
| |
| * [[Myofibroblastic tumors]]
| |
| * [[Myophosphorylase deficiency]]
| |
| * [[Müllerian aplasia]]
| |
| * [[Münchausen syndrome by proxy]]
| |
| * [[Neural tube defect, folate-sensitive]]
| |
| * [[Neural tube defects X linked]]
| |
| * [[Neuraminidase beta-galactosidase deficiency]]
| |
| * [[Neuroaxonal dystrophy, late infantile]]
| |
| * [[Neurofibromatosis, Type IV, of Riccardi]]
| |
| * [[Nevus sebaceus of Jadassohn]]
| |
| * [[Niemann-Pick disease type D]]
| |
| * [[Niemann–Pick C1 disease]]
| |
| * [[Niemann–Pick C2 disease]]
| |
| * [[Norman–Roberts lissencephaly syndrome]]
| |
| * [[Nystagmus with congenital zonular cataract]]
| |
| * [[Ockelbo disease]]
| |
| * [[Ocular histoplasmosis]]
| |
| * [[Oculo dento digital dysplasia]]
| |
| * [[Oculo facio cardio dental syndrome]]
| |
| * [[Oculo-auriculo-vertebral dysplasia]]
| |
| * [[Oligophernia]] | | * [[Oligophernia]] |
| * [[Omodysplasia type 2]] | | * [[Omodysplasia type 2]] |
| * [[Ophthalmophobia]] | | * [[Ophthalmophobia]] |
| * [[Opioid dependence]]
| |
| * [[Opitz syndrome]]
| |
| * [[Oral facial digital syndrome]]
| |
| * [[Oral facial digital syndrome type 3]]
| |
| * [[Orotic aciduria hereditary]] | | * [[Orotic aciduria hereditary]] |
| * [[Orotic aciduria purines-pyrimidines]]
| |
| * [[Osebold–Remondini syndrome]]
| |
| * [[Osmed syndrome]]
| |
| * [[Osteoglophonic dwarfism]]
| |
| * [[Otofaciocervical syndrome]]
| |
| * [[PIRA]] | | * [[PIRA]] |
| * [[Pachyonychia congenita Jackson–Lawler type]]
| |
| * [[Palmitoyl-protein thioesterase deficiency]]
| |
| * [[Panthophobia]] | | * [[Panthophobia]] |
| * [[Parasitophobia]] | | * [[Parasitophobia]] |
| * [[Paroxysmal dystonic choreoathetosis]]
| |
| * [[Partial agenesis of corpus callosum]]
| |
| * [[Parturiphobia]] | | * [[Parturiphobia]] |
| * [[Passive-aggressive personality disorder]]
| |
| * [[Pemphigus vulgaris, familial]]
| |
| * [[Perceptual disorder]] | | * [[Perceptual disorder]] |
| * [[Pericardial constriction with growth failure]]
| |
| * [[Perilymphatic fistula]]
| |
| * [[Peripheral nervous disorder]] | | * [[Peripheral nervous disorder]] |
| * [[Pharmacophobia]] | | * [[Pharmacophobia]] |
| * [[Phenylketonuria type II]] | | * [[Phenylketonuria type II]] |
| * [[Phenylketonuric embryopathy]]
| |
| * [[Phocomelia syndrome]]
| |
| * [[Phosphoglucomutase deficiency]]
| |
| * [[Phosphomannoisomerase deficiency]]
| |
| * [[Phytanic acid oxidase deficiency]]
| |
| * [[Pie Torcido]] | | * [[Pie Torcido]] |
| * [[Pierre Marie cerebellar ataxia]]
| |
| * [[Pili canulati]] | | * [[Pili canulati]] |
| * [[Pitt–Rogers–Danks syndrome]]
| |
| * [[Pituitary dwarfism 1]]
| |
| * [[Platelet disorder]]
| |
| * [[Pneumonia, eosinophilic]]
| |
| * [[Poikiloderma congenital with bullae Weary type]] | | * [[Poikiloderma congenital with bullae Weary type]] |
| * [[Poikiloderma hereditary acrokeratotic Weary type]] | | * [[Poikiloderma hereditary acrokeratotic Weary type]] |
| * [[Poikiloderma of Rothmund–Thomson]]
| |
| * [[Polyarthritis, systemic]]
| |
| * [[Polycystic kidney disease, adult type]]
| |
| * [[Polycystic kidney disease, recessive type]]
| |
| * [[Polycystic kidney disease, type 1]]
| |
| * [[Polycystic kidney disease, type 2]]
| |
| * [[Polycystic kidney disease, type 3]]
| |
| * [[Polycystic ovarian disease, familial]]
| |
| * [[Polydactyly postaxial]]
| |
| * [[Polydactyly preaxial type 1]]
| |
| * [[Polyglucosan body disease, adult]]
| |
| * [[Polyomavirus Infections]] | | * [[Polyomavirus Infections]] |
| * [[Polyposis, hamartomatous intestinal]]
| |
| * [[Porphyria cutanea tarda, familial type]]
| |
| * [[Porphyria cutanea tarda, sporadic type]]
| |
| * [[Porphyria, Ala-D]]
| |
| * [[Porphyria, hereditary coproporphyria]]
| |
| * [[Portal thrombosis]]
| |
| * [[Portuguese type amyloidosis]]
| |
| * [[Positive rheumatoid factor polyarthritis]]
| |
| * [[Posterior tibial tendon rupture]]
| |
| * [[Posterior valve urethra]] | | * [[Posterior valve urethra]] |
| * [[Potter disease type 1]]
| |
| * [[Potter disease, type 3]]
| |
| * [[Potter syndrome dominant type]]
| |
| * [[Poxviridae disease]]
| |
| * [[Precocious puberty, gonadotropin-dependent]]
| |
| * [[Pregnancy toxemia /hypertension]]
| |
| * [[Premature aging]]
| |
| * [[Primary craniosynostosis]]
| |
| * [[Primary granulocytic sarcoma]]
| |
| * [[Primary malignant lymphoma]]
| |
| * [[Primary muscular atrophy]] | | * [[Primary muscular atrophy]] |
| * [[Primary tubular proximal acidosis]]
| |
| * [[Primerose syndrome]]
| |
| * [[Primordial microcephalic dwarfism Crachami type]]
| |
| * [[Prinzmetal's variant angina]]
| |
| * [[Proconvertin deficiency, congenital]]
| |
| * [[Progeroid syndrome De Barsy type]]
| |
| * [[Promoter (biology)]]
| |
| * [[Protein–energy malnutrition]]
| |
| * [[Proximal spinal muscular atrophy]]
| |
| * [[Pseudo-Gaucher disease]]
| |
| * [[Psychophysiologic disorders]]
| |
| * [[Pterygium (eye)]]
| |
| * [[Ptosis (disambiguation)]] | | * [[Ptosis (disambiguation)]] |
| * [[Pulmonary fibrosis /granuloma]]
| |
| * [[Pulmonary hypertension, secondary]]
| |
| * [[Purpura, Schönlein–Henoch]]
| |
| * [[Purpura, thrombotic thrombocytopenic]]
| |
| * [[Pyridoxine deficit]]
| |
| * [[Pyrimidinemia familial]]
| |
| * [[Quincke's edema]] | | * [[Quincke's edema]] |
| * [[Radiation syndromes]]
| |
| * [[Radio-ulnar synostosis type 2]]
| |
| * [[Rambam Hasharon syndrome]]
| |
| * [[Reactive attachment disorder of early childhood]]
| |
| * [[Reactive attachment disorder of infancy]]
| |
| * [[Rectal neoplasm]] | | * [[Rectal neoplasm]] |
| * [[Rectosigmoid neoplasm]] | | * [[Rectosigmoid neoplasm]] |
| * [[Reifenstein syndrome]]
| |
| * [[Renal dysplasia limb defects]]
| |
| * [[Renal dysplasia mesomelia radiohumeral fusion]] | | * [[Renal dysplasia mesomelia radiohumeral fusion]] |
| * [[Renal tubular acidosis, distal]]
| |
| * [[Respiratory distress syndrome, adult]]
| |
| * [[Retina disorder]] | | * [[Retina disorder]] |
| * [[Retinopathy, diabetic]]
| |
| * [[Retinoschisis, X-linked]]
| |
| * [[Retinoschisis, juvenile]]
| |
| * [[Rhabdomyosarcoma, alveolar]]
| |
| * [[Rhabdomyosarcoma, embryonal]]
| |
| * [[Romberg hemi-facial atrophy]]
| |
| * [[Rosenberg–Chutorian syndrome]]
| |
| * [[Roussy–Levy hereditary areflexic dystasia]]
| |
| * [[SSADH (succinic semialdehyde dehydrogenase deficiency)]]
| |
| * [[SSPE (subacute sclerosing panencephalitis)]]
| |
| * [[Sacral defect anterior sacral meningocele]]
| |
| * [[Saito-Kuba-Tsuruta syndrome]]
| |
| * [[Sakati syndrome]]
| |
| * [[Salivary disorder]] | | * [[Salivary disorder]] |
| * [[Sarcoma, granulocytic]]
| |
| * [[Schamberg's disease pigmentation disorder]]
| |
| * [[Schinzel syndrome]]
| |
| * [[Scoliosis as part of NF]] | | * [[Scoliosis as part of NF]] |
| * [[Seafood poisoning]] | | * [[Seafood poisoning]] |
| * [[Sex chromosome disorders (disambiguation)]]
| |
| * [[Shaver's disease]]
| |
| * [[Short rib-polydactyly syndrome, Beermer type]]
| |
| * [[Short rib-polydactyly syndrome, Saldino-Noonan type]]
| |
| * [[Short rib-polydactyly syndrome, Verma-Naumoff type]]
| |
| * [[Short syndrome]]
| |
| * [[Shwachman–Bodian–Diamond syndrome]]
| |
| * [[Shy–Drager syndrome]]
| |
| * [[Sialidosis type 1 and 3]]
| |
| * [[Sialuria, French type]]
| |
| * [[Sideroblastic anemia, autosomal]]
| |
| * [[Skin peeling syndrome]]
| |
| * [[Smith–Martin–Dodd syndrome]]
| |
| * [[Spastic paraplegia type 1, X-linked]] | | * [[Spastic paraplegia type 1, X-linked]] |
| * [[Spastic paraplegia type 2, X-linked]]
| |
| * [[Spastic paraplegia type 3, dominant]]
| |
| * [[Spastic paraplegia type 4, dominant]]
| |
| * [[Spastic paraplegia type 5A, recessive]] | | * [[Spastic paraplegia type 5A, recessive]] |
| * [[Spastic paraplegia type 5B, recessive]]
| |
| * [[Spastic paraplegia type 6, dominant]] | | * [[Spastic paraplegia type 6, dominant]] |
| * [[Spastic paraplegia, familial]]
| |
| * [[Spielmeyer–Vogt disease]]
| |
| * [[Spinal muscular atrophy with pontocerebellar hypoplasia]]
| |
| * [[Spinal muscular atrophy with respiratory distress type 1]] | | * [[Spinal muscular atrophy with respiratory distress type 1]] |
| * [[Spleen neoplasm]]
| |
| * [[Split-hand deformity]] | | * [[Split-hand deformity]] |
| * [[Spondyloepiphyseal dysplasia, congenital type]]
| |
| * [[Spondylometaphyseal dysplasia]]
| |
| * [[St. Anthony's fire (disambiguation)]] | | * [[St. Anthony's fire (disambiguation)]] |
| * [[Stein–Leventhal syndrome]]
| |
| * [[Stickler syndrome, type 1]]
| |
| * [[Stomach cancer, familial]]
| |
| * [[Stratton–Parker syndrome]]
| |
| * [[Streptococcus, Group B]]
| |
| * [[Strudwick syndrome]]
| |
| * [[Strumpell–Lorrain disease]]
| |
| * [[Strychnine poisoning]]
| |
| * [[Stuccokeratosis]] | | * [[Stuccokeratosis]] |
| * [[Subacute sclerosing leucoencephalitis]]
| |
| * [[Sucrase-isomaltase deficiency]]
| |
| * [[Syncopal tachyarythmia]]
| |
| * [[Syndactyly type 2]]
| |
| * [[Synovial cancer]]
| |
| * [[Synovialosarcoma]] | | * [[Synovialosarcoma]] |
| * [[Syphilis embryopathy]]
| |
| * [[Syringomas]] | | * [[Syringomas]] |
| * [[T-Lymphocytopenia]]
| |
| * [[Taybi–Linder syndrome]]
| |
| * [[Temporomandibular joint dysfunction (TMJ)]]
| |
| * [[Tethered spinal cord disease]]
| |
| * [[Thalamic syndrome]]
| |
| * [[Thiolase deficiency]]
| |
| * [[Thymus neoplasm]]
| |
| * [[Todd's syndrome]]
| |
| * [[Toluene antenatal infection]]
| |
| * [[Toni–Fanconi syndrome]]
| |
| * [[Touraine–Solente–Golé syndrome]]
| |
| * [[Toxoplasmosis, congenital]]
| |
| * [[Transplacental infections]]
| |
| * [[Triatrial heart]]
| |
| * [[Trichofolliculloma]] | | * [[Trichofolliculloma]] |
| * [[Trichomalacia]] | | * [[Trichomalacia]] |
| * [[Triplo X Syndrome]]
| |
| * [[Trophoblastic Neoplasms (gestational trophoblastic disease)]]
| |
| * [[Trueb–Burg–Bottani syndrome]]
| |
| * [[Trypanophobia]] | | * [[Trypanophobia]] |
| * [[Tuberous Sclerosis, type 1]]
| | {{div col end}} |
| * [[Tuberous Sclerosis, type 2]]
| | [[Category:Diseases]] |
| * [[Tucker syndrome]]
| | [[Category:Lists]] |
| * [[Turner–Kieser syndrome]]
| | [[Category:Wanted articles]] |
| * [[Ulbright–Hodes syndrome]]
| |
| * [[Upshaw–Schülman syndrome]]
| |
| * [[Urban–Schosser–Spohn syndrome]]
| |
| * [[Uridine monophosphate synthetase deficiency]]
| |
| * [[Valinemia]]
| |
| * [[Van Maldergem–Wetzburger–Verloes syndrome]]
| |
| * [[Varadi–Papp syndrome]]
| |
| * [[Vas deferens, congenital bilateral aplasia of]]
| |
| * [[Vein of Galen aneurysmal dilatation]]
| |
| * [[Velopharyngeal incompetence]]
| |
| * [[Vertical talus]]
| |
| * [[Von Recklinghausen disease]]
| |
| * [[Waardenburg anophthalmia syndrome]]
| |
| * [[Wagner–Stickler syndrome]]
| |
| * [[Warburg–Thomsen syndrome]]
| |
| * [[Warman–Mulliken–Hayward syndrome]]
| |
| * [[Weber–Sturge–Dimitri syndrome]]
| |
| * [[Weismann–Netter–Stuhl syndrome]]
| |
| * [[Weissenbacher–Zweymuller syndrome]]
| |
| * [[Werdnig–Hoffmann disease]]
| |
| * [[Westerhof–Beemer–Cormane syndrome]]
| |
| * [[Wheat hypersensitivity]]
| |
| * [[Whitaker syndrome]]
| |
| * [[Woolly hair autosomal recessive]]
| |
| * [[Wooly hair syndrome]]
| |
