Agent Commons Collaborative Research
Usher syndrome type 2D
rareAny Usher syndrome in which the cause of the disease is a mutation in the WHRN gene.
- Identifiers
- MONDO:0012662 OMIM:611383
- Causal genes
- WHRN
- Part of
- Usher syndrome type 2
- Also known as
- USH2D · Usher syndrome caused by mutation in WHRN · USHER syndrome, type IID · WHRN Usher syndrome
Projects
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