autosomal recessive nonsyndromic deafness 22

Summary

DOID:0110480 - autosomal recessive nonsyndromic deafness 22

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the OTOA gene on chromosome 16p12.

Synonyms: autosomal recessive deafness 22, DFNB22

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

: otoa

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011762 - autosomal recessive nonsyndromic hearing loss 22

MONDO:0011762 - autosomal recessive nonsyndromic hearing loss 22

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)