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created at 2021-12-22 03:08:20 UTC
updated at 2021-12-22 07:06:09 UTC
MONDO_bioport_pref_name
183,974 entries
Label
Id
autosomal dominant retinal vasculopathy with cerebral leukodystrophy 8641
hereditary vascular retinopathy 8641
occlusions, mesenteric vascular D008641
retinopathy, vascular, with cerebral and renal involvement and Raynaud and migraine phenomena 8641
retinal vasculopathy with cerebral leukodystrophy 8641
vasculopathy, retinal, with cerebral leukodystrophy 8641
vasculopathy, retinal, with cerebral leukodystrophy; RVCL http://purl.obolibrary.org/obo/MONDO_0008641
retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations 8641