Usher syndrome type 1C (Q32143522)
Usher syndrome type 1 that has material basis in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15
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aliases Usher syndrome type I Acadian variety
USH1C
Usher syndrome type IC
Usher Syndrome, Type I, Acadian Variety
USHER SYNDROME, TYPE IC
Usher syndrome, Acadian variety
Usher syndrome, type 1C
USHER SYNDROME, TYPE IC; USH1C
description Usher syndrome type 1 that has material basis in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15

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