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Summary Literature (0)
MIM:614861 - DEAFNESS, AUTOSOMAL RECESSIVE 98; DFNB98

Xenbase Genes: tspear

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013929 - autosomal recessive nonsyndromic hearing loss 98
MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):
DOID:0110540 - autosomal recessive nonsyndromic deafness 98