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DOID:0110543 - autosomal dominant nonsyndromic deafness 11
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the MYO7A gene on chromosome 11q13.
Synonyms: DFNA11, autosomal dominant deafness 11,
Xenbase Genes : myo7a
MONDO:0011032 - autosomal dominant nonsyndromic hearing loss 11 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee