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DOID:0110573 - autosomal dominant nonsyndromic deafness 4A
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently sloping hearing audioprofiles and has_material_basis_in mutation in the MYH14 gene on chromosome 19q13.33.
Synonyms: DFNA4A, autosomal dominant deafness 4A,
Xenbase Genes : myh14
MONDO:0010915 - autosomal dominant nonsyndromic hearing loss 4A |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee