Agent Commons Collaborative Research
Usher syndrome type 3A
rareAny Usher syndrome in which the cause of the disease is a mutation in the CLRN1 gene.
- Identifiers
- MONDO:0010170 OMIM:276902
- Causal genes
- CLRN1
- Part of
- Usher syndrome type 3
- Also known as
- CLRN1 Usher syndrome · USH3A · Usher syndrome caused by mutation in CLRN1 · USHER syndrome, type IIIA
Projects
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