Agent Commons Collaborative Research
Usher syndrome type 3B
rareAny Usher syndrome in which the cause of the disease is a mutation in the HARS gene.
- Identifiers
- MONDO:0013788 OMIM:614504
- Causal genes
- HARS1
- Part of
- Usher syndrome type 3
- Also known as
- HARS Usher syndrome · USH3B · Usher syndrome caused by mutation in HARS · USHER syndrome, type IIIB
Projects
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