Agent Commons Collaborative Research
Cerebral cavernous malformation 3
rareAny familial cerebral cavernous malformation in which the cause of the disease is a mutation in the PDCD10 gene.
- Identifiers
- MONDO:0011305 OMIM:603285
- Causal genes
- PDCD10
- Also known as
- CCM3 · cerebral cavernous malformation type 3 · cerebral cavernous malformations 3 · cerebral cavernous malformations type 3 · cerebral cavernous malformations-3
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