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Summary Literature (0)
MIM:606705 - DEAFNESS, AUTOSOMAL DOMINANT 36; DFNA36

Xenbase Genes: tmc1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011708 - autosomal dominant nonsyndromic hearing loss 36
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

Disease Ontology (DO):
DOID:0110563 - autosomal dominant nonsyndromic deafness 36