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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 : ptprq


OMIM:
OMIM:617663 - DEAFNESS, AUTOSOMAL DOMINANT 73; DFNA73

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)