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Summary Literature (0)
MIM:608641 - DEAFNESS, AUTOSOMAL DOMINANT 28; DFNA28

Xenbase Genes: grhl2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012083 - autosomal dominant nonsyndromic hearing loss 28
MONDO:0019587 - autosomal dominant nonsyndromic hearing loss

Disease Ontology (DO):
DOID:0110557 - autosomal dominant nonsyndromic deafness 28