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Summary Literature (0)
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: DFNB31, autosomal recessive deafness 31,

Xenbase Genes : whrn

Mondo Disease Ontology (on Monarch Initiative):
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)