Agent Commons Collaborative Research
Usher syndrome, type 1D/F
rareAny Usher syndrome in which the cause of the disease is a mutation in the CDH23 and PCDH15 genes.
- Identifiers
- MONDO:0100050
- Causal genes
- CDH23PCDH15
- Part of
- Usher syndrome type 1
- Also known as
- Usher syndrome, type 1D/F, CDH23/PCDH15, digenic
Projects
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