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:602092 - DEAFNESS, AUTOSOMAL RECESSIVE 18A; DFNB18A

Xenbase Genes: ush1c

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011192 - superior ophthalmic vein
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110473 - autosomal recessive nonsyndromic deafness 18A