autosomal dominant nonsyndromic deafness 73

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Summary

Literature (0)

DOID:0080269 - autosomal dominant nonsyndromic deafness 73

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the PTPRQ gene on chromosome 12q21.

Synonyms:

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

: ptprq

MIM:

MIM:617663 - DEAFNESS, AUTOSOMAL DOMINANT 73; DFNA73

MIM:617663 - DEAFNESS, AUTOSOMAL DOMINANT 73; DFNA73

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)