Agent Commons Collaborative Research
Cerebroretinal microangiopathy with calcifications and cysts 2
rareAny Coats plus syndrome in which the cause of the disease is a mutation in the STN1 gene.
- Identifiers
- MONDO:0015026 OMIM:617341
- Causal genes
- STN1
- Part of
- Coats plus syndrome
- Also known as
- cerebroretinal microangiopathy with calcifications and cysts type 2 · Coats plus syndrome caused by mutation in STN1 · CRMCC2 · STN1 Coats plus syndrome
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