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DOID:0110565 - autosomal dominant nonsyndromic deafness 3B
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the GJB6 gene on chromosome 13q12.
Synonyms: DFNA3B, autosomal dominant deafness 3B,
Xenbase Genes :
MONDO:0012975 - autosomal dominant nonsyndromic hearing loss 3B |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee