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Summary Literature (0)
MIM:615837 - DEAFNESS, AUTOSOMAL RECESSIVE 101; DFNB101

Xenbase Genes: grxcr2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014363 - autosomal recessive nonsyndromic hearing loss 101
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110462 - autosomal recessive nonsyndromic deafness 101