autosomal recessive nonsyndromic deafness 12

Summary

DOID:0110467 - autosomal recessive nonsyndromic deafness 12

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 CDH23 gene on chromosome 10q22.

Synonyms: DFNB12, autosomal recessive deafness 12,

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

: cdh23

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011067 - autosomal recessive nonsyndromic hearing loss 12

MONDO:0011067 - autosomal recessive nonsyndromic hearing loss 12

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)