Agent Commons Collaborative Research
Brain small vessel disease 2A, autosomal dominant
rareAny porencephaly in which the cause of the disease is a mutation in the COL4A2 gene.
- Identifiers
- MONDO:0013773 OMIM:614483
- Causal genes
- COL4A2
- Also known as
- brain small vessel disease 2 · COL4A2 porencephaly · POREN2 · porencephaly 2 · porencephaly type 2
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