autosomal dominant retinal vasculopathy with cerebral leukodystrophy (Q18209717)

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human disease
  • Cerebroretinal Vasculopathy
  • AD-RVCL
  • Hereditary Vascular Retinopathy
  • Grand Kaine Fulling syndrome
  • retinal vasculopathy and cerebral leukoencephalopathy
  • Retinal vasculopathy with cerebral leukodystrophy
  • Grand-Kaine-Fulling syndrome
  • VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL
  • RVCL
  • ADRVCL
  • Cerebroretinal Vasculopathy, Hereditary
  • VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY
  • Retinopathy, vascular, with cerebral and renal involvement and Raynaud and migraine phenomena
  • CRV
  • Autosomal Dominant Retinal Vasculopathy with Cerebral Leukodystrophy
  • HVR
  • RVCL-S
  • retinal vasculopathy with cerebral leukodystrophy
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Language Label Description Also known as
English
autosomal dominant retinal vasculopathy with cerebral leukodystrophy
human disease
  • Cerebroretinal Vasculopathy
  • AD-RVCL
  • Hereditary Vascular Retinopathy
  • Grand Kaine Fulling syndrome
  • retinal vasculopathy and cerebral leukoencephalopathy
  • Retinal vasculopathy with cerebral leukodystrophy
  • Grand-Kaine-Fulling syndrome
  • VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL
  • RVCL
  • ADRVCL
  • Cerebroretinal Vasculopathy, Hereditary
  • VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY
  • Retinopathy, vascular, with cerebral and renal involvement and Raynaud and migraine phenomena
  • CRV
  • Autosomal Dominant Retinal Vasculopathy with Cerebral Leukodystrophy
  • HVR
  • RVCL-S
  • retinal vasculopathy with cerebral leukodystrophy

Statements

Identifiers

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9B78.0
Retinal vasculopathy and cerebral leukodystrophy
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