autosomal recessive nonsyndromic deafness 31

Summary

DOID:0110490 - autosomal recessive nonsyndromic deafness 31

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the WHRN gene on chromosome 9q32.

Synonyms: autosomal recessive deafness 31, DFNB31

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

: whrn

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011767 - autosomal recessive nonsyndromic hearing loss 31

MONDO:0011767 - autosomal recessive nonsyndromic hearing loss 31

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)