autosomal dominant nonsyndromic deafness 65

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Summary

Literature (0)

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: autosomal dominant deafness 65, DFNA65

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: tbc1d24, tbc1d24.2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014470 - autosomal dominant nonsyndromic hearing loss 65

MONDO:0014470 - autosomal dominant nonsyndromic hearing loss 65

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant nonsyndromic deafness (is_a)