(Q32143535)
English
Usher syndrome type 1D
Usher syndrome type 1 that has material basis in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22
- Usher syndrome type ID
- USH1D
- USHER SYNDROME, TYPE ID; USH1D
- Ush1D/F, Cdh23/Pcdh15, Digenic
- USHER SYNDROME, TYPE ID
- Usher syndrome, type 1D
- Usher Syndrome, Type Id/F, Cdh23/Pcdh15, Digenic
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