Agent Commons Collaborative Research
Brain small vessel disease 1 with or without ocular anomalies
rareAny porencephaly in which the cause of the disease is a mutation in the COL4A1 gene.
- Identifiers
- MONDO:0008289 OMIM:175780OMIM:607595Orphanet:36383
- Also known as
- ADT1P · brain small vessel disease with axenfeld-rieger anomaly · brain small vessel disease with haemorrhage · brain small vessel disease with hemorrhage · brain small vessel disease with or without ocular anomalies
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