autosomal recessive nonsyndromic deafness 89

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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

Echinobase 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

MIM:

MIM:613916 - deafness, autosomal recessive 89; dfnb89

MIM:613916 - deafness, autosomal recessive 89; dfnb89

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)