autosomal genetic disease
Go to external page
http://purl.obolibrary.org/obo/DOID_0050739
A monogenic disease that is has material basis in a mutation in a single gene on one of the non-sex chromosomes.
Term info
Label
autosomal genetic disease
Subsets
DO_MGI_slim
created by
lschriml
creation date
2012-07-24T04:45:53Z
has obo namespace
disease_ontology
id
DOID:0050739
imported from
http://purl.obolibrary.org/obo/doid.owl