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MIM:609439 - DEAFNESS, AUTOSOMAL RECESSIVE 48; DFNB48
Xenbase Genes: cib2
Human Disease Resource: OMIM
MONDO:0012273 - autosomal recessive nonsyndromic hearing loss 48 |
MONDO:0019588 - hearing loss, autosomal recessive |
DOID:0110505 - autosomal recessive nonsyndromic deafness 48 |