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:600060 - DEAFNESS, AUTOSOMAL RECESSIVE 2; DFNB2

Xenbase Genes: myo7a

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010807 - autosomal recessive nonsyndromic hearing loss 2
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110477 - autosomal recessive nonsyndromic deafness 2