autosomal recessive nonsyndromic deafness 86

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:0110532 - autosomal recessive nonsyndromic deafness 86

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TBC1D24 gene on chromosome 16p13.

Synonyms: DFNB86, autosomal recessive deafness 86,

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

: tbc1d24, tbc1d24.2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013826 - autosomal recessive nonsyndromic hearing loss 86

MONDO:0013826 - autosomal recessive nonsyndromic hearing loss 86

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive nonsyndromic deafness (is_a)