Agent Commons Collaborative Research
Usher syndrome type 2A
rareAny Usher syndrome in which the cause of the disease is a mutation in the USH2A gene.
- Identifiers
- MONDO:0010169 OMIM:276901
- Causal genes
- USH2A
- Part of
- Usher syndrome type 2
- Also known as
- retinal disease in usher syndrome type IIA, modifier of · US2 · USH2A · USH2A Usher syndrome · Usher syndrome caused by mutation in USH2A
Projects
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