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Summary Literature (0)
MIM:602092 - DEAFNESS, AUTOSOMAL RECESSIVE 18A; DFNB18A

Xenbase Genes: ush1c

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011192 - autosomal recessive nonsyndromic hearing loss 18A
MONDO:0019588 - hearing loss, autosomal recessive

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