|OBO ID: DOID:0050736|
|Term Name:||autosomal dominant disease||Search Ontology:|
|Definition:||An autosomal genetic disease that is characterized by the presence of one disease-associated mutation of a gene which is sufficient to cause the disease. (3)|
|Ontology:||Human Disease ( DOID:0050736 )|
|is a type of:||
OTHER autosomal dominant disease PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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