autosomal recessive nonsyndromic deafness 68

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:0110519 - autosomal recessive nonsyndromic deafness 68

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the S1PR2 gene on chromosome 19p13.

Synonyms: autosomal recessive deafness 68, DFNB68

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

: s1pr2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012485 - autosomal recessive nonsyndromic hearing loss 68

MONDO:0012485 - autosomal recessive nonsyndromic hearing loss 68

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)