autosomal dominant
90 results
1 - 90
autosomal dominant- gene
- dominant optic atrophy and deafness
- Howel-Evans syndrome
- tremor
- mesomelic dwarfism
- Muir-Torre syndrome
- Fahr, Karl Theodor
- Parrot, Joseph Marie Jules
- Blau syndrome
- fever
- Beckwith-Wiedemann syndrome
- basal cell nevus syndrome
- Fryns syndrome
- Weyer acrofacial dysostosis
- dystrophy
- dardarin
- coproporphyria, hereditary coproporphyria
- proprotein convertase subtilisin kexin 9
- Pfeiffer, Richard F.
- dystonia
- Loeys-Dietz syndrome
- warfarin resistance syndrome
- hyperthermia
- Darier, Ferdinand Jean
- keratosis
- epidermal nevus syndrome
- Schnyder crystalline dystrophy
- dyskeratosis congenita
- telangiectasia, telangiectasis
- Birt-Hogg-Dubé syndrome
- facies
- neurofibromatosis
- Brugada syndrome
- Amish lethal microcephaly
- disease
- Hailey-Hailey disease
- arthrochalasia
- startle syndrome
- hyperimmunoglobulinemia E syndrome
- Van der Woude syndrome
- Bethlem myopathy
- Noonan syndrome
- neuroferritinopathy
- stomatocytosis, hereditary
- atrophy
- neuropathy
- mutation
- Hajdu-Cheney syndrome
- hyperekplexia, hyperexplexia
- Cornelia de Lange syndrome
- rippling muscle disease
- myelokathexis
- Kniest dysplasia
- May-Hegglin anomaly
- porphyria
- diabetes
- Andersen syndrome, Andersen-Tawil syndrome
- Kabuki syndrome, Kabuki make up syndrome
- hereditary xerocytosis
- arachnodactyly
- resistance to thyroid hormone
- familial adenomatous polyposis
- Gerstmann-Sträussler-Scheinker syndrome
- angioedema
- ichthyosis
- alpha granule deficiency syndrome
- sleep-phase syndrome
- Pelger-Huët anomaly
- progeria
- osteopetrosis
- Liddle syndrome
- Wolff-Parkinson-White syndrome
- Crouzon disease
- Huntington disease
- hyperlipoproteinemia
- Willebrand disease, von Willebrand disease
- Machado-Joseph disease
- polycystic kidney disease
- osteogenesis, osteogeny
- Marfan syndrome
- Alexander disease
- Lynch syndrome
- Waardenburg syndrome
- cardiomyopathy
- Gilbert syndrome
- scoliosis
- pheochromocytoma