autosomal recessive nonsyndromic deafness 89

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary

Literature (0)

DOID:0110534 - autosomal recessive nonsyndromic deafness 89

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the KARS gene on chromosome 16q23.

Synonyms: autosomal recessive deafness 89, DFNB89

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

: kars1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013489 - autosomal recessive nonsyndromic hearing loss 89

MONDO:0013489 - autosomal recessive nonsyndromic hearing loss 89

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)