Retinal vasculopathy and cerebral leukodystrophy (Q41772): Difference between revisions
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Linked ICD 10: H35 / rank | |||||||||||||||
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Latest revision as of 08:03, 13 August 2026
Retinal vasculopathy and cerebral leukodystrophy is an inherited group of small vessel diseases comprised of cerebroretinal vasculopathy, hereditary vascular retinopathy and hereditary endotheliopathy with retinopathy, nephropathy and stroke (HERNS); all exhibiting progressive visual impairment as well as variable cerebral dysfunction.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 9B78.0 |
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| English | Retinal vasculopathy and cerebral leukodystrophy |
Retinal vasculopathy and cerebral leukodystrophy is an inherited group of small vessel diseases comprised of cerebroretinal vasculopathy, hereditary vascular retinopathy and hereditary endotheliopathy with retinopathy, nephropathy and stroke (HERNS); all exhibiting progressive visual impairment as well as variable cerebral dysfunction. |
Statements
CID11:9B78.0
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dki-india-9B78.0
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Concluído
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13 August 2026
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