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Summary Literature (2)
MIM:601072 - DEAFNESS, AUTOSOMAL RECESSIVE 8; DFNB8

Xenbase Genes: tmprss3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010987 - autosomal recessive nonsyndromic hearing loss 8
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110527 - autosomal recessive nonsyndromic deafness 8