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: DFNB68, autosomal recessive deafness 68,

Xenbase Genes : s1pr2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012485 - autosomal recessive nonsyndromic hearing loss 68


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)