Category:Genetic Disorders
From WikiMD's Medical Encyclopedia
This is a category page. It lists all of the pages in category "Genetic Disorders" as well as all subcategories of category "Genetic Disorders" if any exist.
Pages in category "Genetic Disorders"
The following 200 pages are in this category, out of 224 total.
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B
C
- Calvarial hyperostosis
- Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
- Cataract anterior polar dominant
- Caudal regression syndrome
- CE
- Channelopathy
- Chemke–Oliver–Mallek syndrome
- CHST14
- Ciliary discoordination, due to random ciliary orientation
- CLCN1
- Cleft lip palate ectrodactyly
- Cleft lip palate mental retardation corneal opacity
- Cleft lower lip cleft lateral canthi chorioretinal
- Cole–Carpenter syndrome
- Collagen, type VII, alpha 1
- Congenital heart disease radio ulnar synostosis mental retardation
- Congenital hemolytic anemia
- Congenital hyperinsulinism
- Congenital hypoplastic anemia
- Congenital muscular dystrophy
- Congenital myopathy
- Contractures ectodermal dysplasia cleft lip palate
- Cormier–Rustin–Munnich syndrome
- Coxoauricular syndrome
- Cramer–Niederdellmann syndrome
- Craniosynostosis arthrogryposis cleft palate
- Crawfurd syndrome
- Crouzonodermoskeletal syndrome
- Curry–Hall syndrome
D
- De novo mutation
- Deafness conductive stapedial ear malformation facial palsy
- Deafness goiter stippled epiphyses
- Deafness hypospadias metacarpal and metatarsal syndrome
- Defective expression of HLA class 2
- Developmental delay epilepsy neonatal diabetes
- Diaphragmatic defect limb deficiency skull defect
- Dilated cardiomyopathy with ataxia syndrome
- Diprosopus
- Dismutase
- Distal arthrogryposis Moore–Weaver type
- Distal myopathy
- Distal myopathy Markesbery–Griggs type
- Duncan
- Dwarfism tall vertebrae
- Dwarfism thin bones multiple fractures
- Dystrophy
E
- Ectodermal dysplasia arthrogryposis diabetes mellitus
- Ectodermal dysplasia blindness
- Ectodermal dysplasia Margarita type
- Ectodermal dysplasia mental retardation syndactyly
- Ectodermal dysplasia neurosensory deafness
- Ectodermal dysplasia with corkscrew hairs
- Ectrodactyly-polydactyly syndrome
- Elliptocyte
- Epidermolysis bullosa herpetiformis, Dowling–Meara
- Epidermolysis bullosa, junctional, Herlitz–Pearson
- Epidermolytic palmoplantar keratoderma Vorner type
- Epiphyseal dysplasia dysmorphism camptodactyly
- Erythrocyte fragility
- Extrasystoles short stature hyperpigmentation microcephaly
F
G
H
- Harlequin
- Harris platelet syndrome
- Hay–Wells syndrome recessive type
- Heide syndrome
- Hereditary breast–ovarian cancer syndrome
- Hereditary resistance to anti-vitamin K
- Hereditary stomatocytosis
- History of Tay–Sachs disease
- Holoprosencephaly radial heart renal anomalies
- Hyperimmunoglobulin E syndrome
- Hyperplasia of midface
- Hyperprolinemia
- Hypertelorism
- Hypohidrotic ectodermal dysplasia with immune deficiency
- Hypokalemic periodic paralysis
I
K
L
- Laterality defects dominant
- Lethal acantholytic epidermolysis bullosa
- Ligamentous laxity
- Limb girdle syndrome
- Linear hamartoma syndrome
- Lipoid congenital adrenal hyperplasia
- List of biological development disorders
- List of cutaneous conditions caused by mutations in keratins
- List of dental abnormalities associated with cutaneous conditions
- List of disorders included in newborn screening programs
M
- Macular dystrophy
- Mandibulofacial dysostosis-microcephaly syndrome
- Markel–Vikkula–Mulliken syndrome
- Maroteaux–Fonfria syndrome
- Medeira Dennis Donnai syndrome
- Megalencephaly
- Meinecke–Pepper syndrome
- Menke-Hennekam syndrome
- Mental retardation arachnodactyly hypotonia telangiectasia
- Mental retardation contractural arachnodactyly
- Mental retardation dysmorphism hypogonadism diabetes
- Mental retardation nasal hypoplasia obesity genital hypoplasia
- Mental retardation short stature absent phalanges
- Mental retardation short stature deafness genital
- Mental retardation short stature wedge shaped epiphyses
- Michelin tire baby syndrome
- Microdontia hypodontia short stature
- Mild androgen insensitivity syndrome
- Mirror polydactyly-vertebral segmentation-limb defects syndrome
- Moore–Federman syndrome
- Morgani–Turner–Albright syndrome
- Morquio syndrome
- Multiple endocrine neoplasia
- Multiple pterygium syndrome lethal type
O
P
- Palant cleft palate syndrome
- Patel–Bixler syndrome
- Peptidic growth factors deficiency
- Pili torti onychodysplasia
- Platyspondyly amelogenesis imperfecta
- Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
- Polydactyly postaxial dental and vertebral
- Polydactyly postaxial with median cleft of upper lip
- Polydactyly-myopia syndrome
- Polysyndactyly cardiac malformation
- Primary immunodeficiency
- Pseudo-Hurler polydystrophy
- Pseudohermaphroditism mental retardation
- Pterygia mental retardation facial dysmorphism
- Pterygium colli mental retardation digital anomalies
- Pterygium syndrome antecubital
- Pterygium syndrome multiple dominant type
- Pulmonar arterioveinous aneurysm
- Pyruvate carboxylase
R
S
- Sabinas brittle hair syndrome
- Samson–Viljoen syndrome
- Schimke syndrome
- Sener syndrome
- Seow–Najjar syndrome
- Short stature Brussels type
- SMCHD1
- Spherocytosis
- Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome
- Sternal malformation vascular dysplasia association
- Stewart
- Stratton Parker syndrome
- Streeter's dysplasia
