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:610220 - DEAFNESS, AUTOSOMAL RECESSIVE 59; DFNB59

Xenbase Genes: pjvk

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012445 - autosomal recessive nonsyndromic hearing loss 59
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110511 - autosomal recessive nonsyndromic deafness 59