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DOID:0110586 - autosomal dominant nonsyndromic deafness 65
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the TBC1D24 gene on chromosome 16p13.
Synonyms: DFNA65, autosomal dominant deafness 65,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0014470 - autosomal dominant nonsyndromic hearing loss 65 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee