autosomal dominant nonsyndromic deafness 41

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Summary

Literature (0)

DOID:0110567 - autosomal dominant nonsyndromic deafness 41

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat progressive hearing loss and has_material_basis_in mutation in the P2RX2 gene on chromosome 12q24.

Synonyms: DFNA41, autosomal dominant deafness 41,

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

OMIM:

MIM:608224 - deafness, autosomal dominant 41; dfna41

MIM:608224 - deafness, autosomal dominant 41; dfna41

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)