File:Autosomal dominant - en.svg
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File usage
More than 100 pages use this file. The following list shows the first 100 pages that use this file only. A full list is available.
- Medicine:17q12 microdeletion syndrome
- Medicine:2q37 deletion syndrome
- Medicine:Achondroplasia
- Medicine:Acrocephalosyndactylia
- Medicine:Adermatoglyphia
- Medicine:Autosomal dominant porencephaly type I
- Medicine:Autosomal dominant retinal vasculopathy with cerebral leukodystrophy
- Medicine:Axial osteomalacia
- Medicine:Birk-Barel syndrome
- Medicine:Birt–Hogg–Dubé syndrome
- Medicine:Branchio-oto-renal syndrome
- Medicine:CDK13-related disorder
- Medicine:Camurati–Engelmann disease
- Medicine:Cantú syndrome
- Medicine:Cardiofaciocutaneous syndrome
- Medicine:Coffin–Siris syndrome
- Medicine:Costello syndrome
- Medicine:Cryopyrin-associated periodic syndrome
- Medicine:Darier's disease
- Medicine:DiGeorge syndrome
- Medicine:Dunnigan familial partial lipodystrophy
- Medicine:Ectrodactyly–ectodermal dysplasia–cleft syndrome
- Medicine:Erythrokeratodermia variabilis
- Medicine:Familial amyloid polyneuropathy
- Medicine:Familial atrial fibrillation
- Medicine:Fechtner syndrome
- Medicine:Flynn–Aird syndrome
- Medicine:GLUT1 deficiency
- Medicine:Gardner's syndrome
- Medicine:Gastrocutaneous syndrome
- Medicine:Gillespie syndrome
- Medicine:Glut1 deficiency
- Medicine:Hardcastle syndrome
- Medicine:Hay–Wells syndrome
- Medicine:Heart-hand syndromes
- Medicine:Hemifacial hypertrophy
- Medicine:Hereditary diffuse leukoencephalopathy with spheroids
- Medicine:Hereditary hemorrhagic telangiectasia
- Medicine:Hereditary neuralgic amyotrophy
- Medicine:Holt–Oram syndrome
- Medicine:Hypochondroplasia
- Medicine:Ichthyosis with confetti
- Medicine:Idiopathic CD4+ lymphocytopenia
- Medicine:Infantile convulsions and choreoathetosis
- Medicine:Iridogoniodysgenesis, dominant type
- Medicine:Jackson–Weiss syndrome
- Medicine:Jansen's metaphyseal chondrodysplasia
- Medicine:Johnson–McMillin syndrome
- Medicine:Keratolytic winter erythema
- Medicine:Kosaki overgrowth syndrome
- Medicine:Kostmann syndrome
- Medicine:Legius syndrome
- Medicine:Li–Fraumeni syndrome
- Medicine:MASS syndrome
- Medicine:MDP syndrome
- Medicine:Macular hypoplasia
- Medicine:Marfan syndrome
- Medicine:Marshall syndrome
- Medicine:Melkersson–Rosenthal syndrome
- Medicine:Metachondromatosis
- Medicine:Monilethrix
- Medicine:Muckle–Wells syndrome
- Medicine:Naegeli–Franceschetti–Jadassohn syndrome
- Medicine:Nail–patella syndrome
- Medicine:Neurofibromatosis
- Medicine:Noonan syndrome
- Medicine:Oculopharyngeal muscular dystrophy
- Medicine:Okamoto syndrome
- Medicine:Osteopetrosis
- Medicine:PAPA syndrome
- Medicine:PLAID syndrome
- Medicine:Papillorenal syndrome
- Medicine:Parastremmatic dwarfism
- Medicine:Paroxysmal exercise-induced dystonia
- Medicine:Paroxysmal kinesigenic choreoathetosis
- Medicine:Pashayan syndrome
- Medicine:Plantar fibromatosis
- Medicine:Popliteal pterygium syndrome
- Medicine:Primrose syndrome
- Medicine:RAS-associated autoimmune leukoproliferative disorder
- Medicine:Revesz syndrome
- Medicine:Reynolds syndrome
- Medicine:Rombo syndrome
- Medicine:STING-associated vasculopathy with onset in infancy
- Medicine:Saethre–Chotzen syndrome
- Medicine:Scalp–ear–nipple syndrome
- Medicine:Schmitt Gillenwater Kelly syndrome
- Medicine:Severe congenital neutropenia
- Medicine:Sneddon's syndrome
- Medicine:Sorsby's fundus dystrophy
- Medicine:Spinocerebellar ataxia type 6
- Medicine:Spondyloepimetaphyseal dysplasia, Strudwick type
- Medicine:Timothy syndrome
- Medicine:Tracheobronchopathia osteochondroplastica
- Medicine:Treacher Collins syndrome
- Medicine:Tuberous sclerosis
- Medicine:Von Hippel–Lindau disease
- Medicine:Waardenburg syndrome
- Medicine:Warfarin resistance
- Medicine:White sponge nevus
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