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)
MIM:610419 - DEAFNESS, AUTOSOMAL RECESSIVE 68; DFNB68

Xenbase Genes: s1pr2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012485 - autosomal recessive nonsyndromic hearing loss 68
MONDO:0019588 - hearing loss, autosomal recessive