autosomal dominant disease · genetic disease characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease · YYNN

autosomal dominant disease

? TBD

genetic disease characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease

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Subclasses
40

Paroxysmal extreme pain disorder

Rare disorder of abnormal pain sensation

Costello syndrome

Medical condition

Central hypoventilation syndrome

Medical condition

Tuberous sclerosis

Genetic condition causing non-cancerous tumours

Miller–Dieker syndrome

Genetic disorder

Hereditary nonpolyposis colorectal cancer

Autosomal dominant genetic condition associated with a high risk of cancer in the colon

Genetic disorder that causes early aging

Familial male-limited precocious puberty

Medical condition

Familial amyloid polyneuropathy

Medical condition

Fibrodysplasia ossificans progressiva

Disease in which fibrous connective tissue turns into bone

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class of disease

Wikidata