autosomal recessive nonsyndromic deafness 15

Summary

DOID:0110470 - autosomal recessive nonsyndromic deafness 15

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the GIPC3 gene on chromosome 19p13.

Synonyms: autosomal recessive deafness 15, autosomal recessive deafness 72, autosomal recessive deafness 95, DFNB15, DFNB72, DFNB95

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

: gipc3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011160 - autosomal recessive nonsyndromic hearing loss 15

MONDO:0011160 - autosomal recessive nonsyndromic hearing loss 15

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

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

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