(Q32143643)
English
Usher syndrome type 2C
Usher syndrome type 2 that has material basis in homozygous or compound heterozygous mutation in the ADGRV1 gene on chromosome 5q14
- USH2C
- Usher syndrome type IIC
- Usher syndrome, type 2C
- USHER SYNDROME, TYPE IIC
- USHER SYNDROME, TYPE IIC; USH2C
- Usher Syndrome, Type Iib, Formerly
- Usher Syndrome, Type Iib
- Usher Syndrome, Type Iic, Gpr98/Pdzd7, Digenic
Statements
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C153174
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Identifiers
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