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OMIM:603720 - DEAFNESS, AUTOSOMAL RECESSIVE 16; DFNB16
Xenbase Genes: strc
Human Disease Resource: OMIM
MONDO:0011364 - autosomal recessive nonsyndromic hearing loss 16 |
MONDO:0019588 - hearing loss, autosomal recessive |
DOID:0110471 - autosomal recessive nonsyndromic deafness 16 |