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Usher syndrome type 1F
rareA form of Usher syndrome type IF that can be caused by homozygous or compound heterozygous mutation in the protocadherin-15 gene (PCDH15) on chromosome 10q. It is inherited in an autosomal recessive manner.
- Identifiers
- MONDO:0011186 OMIM:602083
- Causal genes
- PCDH15
- Part of
- Usher syndrome type 1
- Also known as
- USH1F · Usher syndrome, type 1F · USHER syndrome, type IF
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