DEAFNESS, AUTOSOMAL RECESSIVE 91; DFNB91

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Summary

Literature (0)

MIM:613453 - DEAFNESS, AUTOSOMAL RECESSIVE 91; DFNB91

Xenbase Genes: serpinb6

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013269 - autosomal recessive nonsyndromic hearing loss 91
MONDO:0019588 - hearing loss, autosomal recessive

MONDO:0013269 - autosomal recessive nonsyndromic hearing loss 91

MONDO:0019588 - hearing loss, autosomal recessive

Disease Ontology (DO):

DOID:0110536 - autosomal recessive nonsyndromic deafness 91

DOID:0110536 - autosomal recessive nonsyndromic deafness 91