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Summary Literature (0)
MIM:608265 - DEAFNESS, AUTOSOMAL RECESSIVE 39; DFNB39

Xenbase Genes: hgf

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012003 - autosomal recessive nonsyndromic hearing loss 39
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110497 - autosomal recessive nonsyndromic deafness 39