|
DOID:0110584 - autosomal dominant nonsyndromic deafness 6
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and low frequency progressive hearing loss and has_material_basis_in mutation in the WFS1 gene on chromosome 4p16.
Synonyms: DFNA14, DFNA38, DFNA6, autosomal dominant deafness 14, autosomal dominant deafness 38, autosomal dominant deafness 6,
Echinobase Genes :
MIM:600965 - deafness, autosomal dominant 6; dfna6 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee