brain small vessel disease 1 with or without ocular anomalies https://www.malacards.org/card/brain_small_vessel_disease_1 https://www.malacards.org/card/brain_small_vessel_disease_1_with_or_without_ocular_anomalies porencephaly, type 1, autosomal dominant porencephaly type 1 Any porencephaly in which the cause of the disease is a mutation in the COL4A1 gene. MESH:C564372 brain small vessel disease with axenfeld-rieger anomaly MONDO:0008289 brain small vessel disease with hemorrhage porencephaly 1 brain small vessel disease with haemorrhage T1P leukoencephalopathy with axenfeld-rieger anomaly OMIM:175780 BSVD1 brain small vessel disease with or without ocular anomalies MEDGEN:1663316 DOID:0090125 GARD:0015107 UMLS:C4755307 porencephaly caused by mutation in COL4A1 BSVD Orphanet:36383 hemiplegia, infantile, with porencephaly MESH:C531642 POREN1 ADT1P COL4A1-related brain small vessel disease with haemorrhage COL4A1 porencephaly OMIM:607595 retinal arteriolar tortuosity, infantile hemiparesis, and leukoencephalopathy, autosomal dominant obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendency familial porencephaly COL4A1-related disorder