Concept information
Preferred term
Dominant hereditary disorder, NOS
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- Aase syndrome
- Acrokeratosis verruciformis of Hopf (disorder)
- Adult onset autosomal dominant leukodystrophy (disorder)
- Albinism-deafness syndrome of Tietz (disorder)
- Andersen Tawil syndrome (disorder)
- Autosomal dominant epidermolysis bullosa simplex (disorder)
- Autosomal dominant familial woolly hair (disorder)
- Autosomal dominant muscular dystrophy not predominantly limb girdle
- Autosomal dominant pseudoxanthoma elasticum (disorder)
- Axenfeld anomaly
- Branchiooculofacial syndrome
- Brugada syndrome (disorder)
- Carpotarsal osteochondromatosis (disorder)
- Centrofacial lentiginosis syndrome
- Charcot-Marie-Tooth disease, type I (disorder)
- Cochleosaccular degeneration and cataract syndrome (disorder)
- Coloboma of macula with brachydactyly type B syndrome (disorder)
- Congenital hereditary endothelial dystrophy,CHED 1 (disorder)
- Currarino triad (disorder)
- Deafness - lymphoedema - leukemia syndrome
- Diabetes mellitus autosomal dominant type II
- Distal myopathy with vocal cord weakness
- Distichiasis-lymphedema syndrome
- Epibulbar lipodermoid, preauricular appendage, polythelia syndrome (disorder)
- Epidermolytic palmoplantar keratoderma of Vorner
- Episodic ataxia (disorder)
- Familial amyloid neuropathy, Finnish type
- Familial amyloid polyneuropathy
- Familial benign pemphigus
- Generalized basaloid follicular hamartoma syndrome (disorder)
- Glucose transporter protein type 1 deficiency syndrome (disorder)
- Granular corneal dystrophy
- Hapnes Boman Skeie syndrome
- Hawkinsinuria (disorder)
- Hemifacial hyperplasia strabismus syndrome
- Hereditary angioneurotic edema with normal C1 esterase inhibitor activity (disorder)
- Hereditary antithrombin III deficiency (disorder)
- Hereditary benign intraepithelial dyskeratosis (disorder)
- Hereditary cavernous hemangioma of brain (disorder)
- Hereditary lymphedema and yellow nails (disorder)
- Hereditary lymphedema type I (disorder)
- Hereditary lymphedema type II (disorder)
- Hereditary neurocutaneous angiomata (disorder)
- Heritable pulmonary arterial hypertension due to BMPR2 mutation (disorder)
- Howel-Evans' syndrome
- Huntington's chorea
- Hypertelorism, preauricular sinus, punctual pits, deafness syndrome (disorder)
- Hypertrophic gastropathy without hypoproteinemia
- IVIC (Instituto Venezolano de Investigaciones Cientificas) syndrome
- Juvenile cataract, microcornea, renal glucosuria syndrome (disorder)
- Juvenile epithelial corneal dystrophy
- Juvenile polyposis syndrome
- Keratoderma with scleroatrophy of the extremities
- Keratosis follicularis
- Kitamura's reticulate acropigmentation
- Li-Fraumeni syndrome (disorder)
- Loeys-Dietz syndrome (disorder)
- Maturity-onset diabetes of the young, type 11
- Maturity onset diabetes of the young, type 1 (disorder)
- Maturity-onset diabetes of the young, type 5 (disorder)
- Microtia, eye coloboma, imperforation of nasolacrimal duct syndrome
- MODY10
- MODY3
- MODY8
- Moebius syndrome (disorder)
- Multiple congenital exostosis
- Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome
- Myotonic dystrophy (disorder)
- Neurofibromatosis, type 1
- Noonan's syndrome
- Odonto-tricho-ungual-digito-palmar syndrome (disorder)
- Osteogenesis imperfecta type I (disorder)
- Polymorphous corneal dystrophy
- Postural orthostatic tachycardia syndrome due to NET (norepinephrine transporter) deficiency
- Progressive palmoplantar keratoderma
- Ptosis and vocal cord paralysis syndrome (disorder)
- Ptosis, strabismus, ectopic pupil syndrome (disorder)
- Reis-Bucklers' corneal dystrophy
- Schnyder crystalline cornea dystrophy (disorder)
- Sensorineural hearing loss, early graying, essential tremor syndrome (disorder)
- Short stature, advanced bone age, early-onset osteoarthritis syndrome
- Steatocystoma multiplex
- Thiel-Behnke corneal dystrophy (disorder)
- Tuberous sclerosis syndrome
- Turcot syndrome
- White sponge nevus of mucosa (disorder)
- Whyte Hemingway carpal tarsal phalangeal osteolyses (disorder)
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/11164009
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