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:607197 - DEAFNESS, AUTOSOMAL RECESSIVE

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0050565 - autosomal recessive nonsyndromic deafness