disease has feature retinal vascular disorder retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/6878 https://github.com/monarch-initiative/mondo/issues/7365 https://rarediseases.info.nih.gov/diseases/10535/hereditary-vascular-retinopathy https://rarediseases.info.nih.gov/diseases/1217/retinal-vasculopathy-with-cerebral-leukodystrophy https://rarediseases.info.nih.gov/diseases/2558/grand-kaine-fulling-syndrome https://www.malacards.org/card/vasculopathy_retinal_with_cerebral_leukoencephalopathy_and_systemic_manifestations retinopathy, vascular, with cerebral and renal involvement and Raynaud and migraine phenomena RVCL hereditary vascular retinopathy retinal vasculopathy and cerebral leukoencephalopathy MESH:C566007 vasculopathy, retinal, with cerebral leukodystrophy OMIM:192315 cerebroretinal vasculopathy, hereditary RVCL-S Orphanet:247691 grand-Kaine-fulling syndrome icd11.foundation:554838792 CRV SCTID:720854004 MONDO:0008641 cerebroretinal vasculopathy NORD:1910 vasculopathy, retinal, with cerebral leukoencephalopathy and systemic manifestations An inherited group of small vessel diseases comprised of cerebroretinal vasculopathy (CRV), hereditary vascular retinopathy (HRV) and hereditary endotheliopathy with retinopathy, nephropathy and stroke (HERNS); all exhibiting progressive visual impairment as well as variable cerebral dysfunction. Editor note: Orphanet:3421 is obsolete in the 2017 edition of ORDO, but the Orphanet website shows as active, see https://github.com/Orphanet/ORDO/issues/1 retinal vasculopathy with cerebral leukodystrophy DOID:0111567 autosomal dominant retinal vasculopathy with cerebral leukodystrophy SCTID:721141004 MEDGEN:348124 grand Kaine fulling syndrome HVR UMLS:C1860518 GARD:0001217 ADRVCL inherited retinal dystrophy obsolete disease of glomerular basement membrane TREX1-related type 1 interferonopathy type 1 interferonopathy of childhood