This is just here as a test because I lose it

Term information

created by

lschriml

creation date

2012-07-24T12:51:47Z

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.

has obo namespace

disease_ontology

id

DOID:0050736

imported from

http://purl.obolibrary.org/obo/doid.owl

Term relations