autosomal dominant nonsyndromic deafness 56

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Summary

Literature (0)

DOID:0110581 - autosomal dominant nonsyndromic deafness 56

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the TNC gene on chromosome 9q33.

Synonyms: DFNA56, autosomal dominant deafness 56,

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

: tnc

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014283 - autosomal dominant nonsyndromic hearing loss 56

MONDO:0014283 - autosomal dominant nonsyndromic hearing loss 56

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

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

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