Also Known As
ADT1PBSVDBSVD1COL4A1 porencephalyCOL4A1-related brain small vessel disease with haemorrhageCOL4A1-related brain small vessel disease with hemorrhageCOL4A1-related familial vascular leukoencephalopathyCOL4A1-related retinal arteriolar tortuosity-infantile hemiparesis-autosomal dominant leukoencephalopathy syndromeT1Pautosomal dominant retinal arteriolar tortuosity, infantile hemiparesis, and leukencephalopathybrain small vessel disease with Axenfeld-Riegar anomalybrain small vessel disease with axenfeld-rieger anomalybrain small vessel disease with haemorrhagebrain small vessel disease with hemorrhagebrain small vessel disease with or without ocular anomalieshemiplegia, infantile, with porencephalyinfantile hemiparesisleukoencephalopathy with axenfeld-rieger anomalyporencephaly 1porencephaly caused by mutation in COL4A1porencephaly type 1retinal arteriolar tortuosity, infantile hemiparesis, and leukoencephalopathy, autosomal dominantPOREN1hemiplegia, infantile, with porencephaly porencephaly, type 1porencephaly, type 1, autosomal dominant