|
DOID:0110558 - autosomal dominant nonsyndromic deafness 2A
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by high frequency progressive hearing loss and has_material_basis_in mutation in the KCNQ4 gene on chromosome 1p34.2.
Synonyms: DFNA2A, autosomal dominant deafness 2A,
Echinobase Genes :
MIM:600101 - deafness, autosomal dominant 2a; dfna2a |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee