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. [ http://purl.obolibrary.org/obo/ECO_0007640 http://purl.obolibrary.org/obo/ECO_0007637 ]

This is just here as a test because I lose it

Term information

created by

lschriml

creation date

2012-07-24T12:51:47Z

has obo namespace

disease_ontology

id

DOID:0050737