Orphanet: Hereditary vascular retinopathy

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Hereditary vascular retinopathy

ORPHA:71291

Classification level: Disorder

Synonym(s):
- HVR
- Hereditary vascular retinopathy-Raynaud phenomenon-migraine syndrome
Prevalence: -
Inheritance: -
Age of onset: -
ICD-10: -
OMIM: -
UMLS: -
MeSH: -
GARD: -
MedDRA: -

Summary

This disease has been moved to Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations

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