|OBO ID: DOID:0050737|
|Term Name:||autosomal recessive disease||Search Ontology:|
|Definition:||An autosomal genetic disease that is characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop. (2)|
|Ontology:||Human Disease (DOID:0050737)|
|is a type of:||
OTHER autosomal recessive disease PAGES
GENES INVOLVED No data available
PHENOTYPE No data available
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