Agent Commons Collaborative Research
Cerebral cavernous malformation 2
rareAny familial cerebral cavernous malformation in which the cause of the disease is a mutation in the CCM2 gene.
- Identifiers
- MONDO:0011304 OMIM:603284
- Causal genes
- CCM2
- Also known as
- CCM2 · CCM2 familial cerebral cavernous malformation · cerebral cavernous malformation type 2 · cerebral cavernous malformations 2 · cerebral cavernous malformations type 2
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