Usher syndrome type 1C (Q32143522)
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Usher syndrome type 1 that has material basis in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15
- 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
Language | Label | Description | Also known as |
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English | Usher syndrome type 1C |
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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