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Summary Literature (0)
MIM:613285 - DEAFNESS, AUTOSOMAL RECESSIVE 25; DFNB25

Xenbase Genes: grxcr1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013210 - autosomal recessive nonsyndromic hearing loss 25
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110483 - autosomal recessive nonsyndromic deafness 25