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Summary Literature (0)
MIM:124480 - DEAFNESS, CONGENITAL, WITH ONYCHODYSTROPHY, AUTOSOMAL DOMINANT; DDOD

Xenbase Genes: atp6v1b2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007420 - autosomal dominant deafness - onychodystrophy syndrome
MONDO:0017922 - obsolete deafness-onychodystrophy syndrome

Disease Ontology (DO):
DOID:0080720 - autosomal dominant congenital deafness with onychodystrophy