PEHO syndrome (Q101728): Difference between revisions
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| Property / Canonical URI: https://id.who.int/icd/entity/976613527 / rank | |||||||||||||||
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CID11:ID_976613527 | |||||||||||||||
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dki-india-ID_976613527 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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Latest revision as of 18:34, 16 August 2026
PEHO (Progressive encephalopathy with Edema, Hypsarrhythmia and Optic atrophy) syndrome is a rare neurodegenerative disorder belonging to the group of infantile progressive encephalopathies.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_976613527 |
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| English | PEHO syndrome |
PEHO (Progressive encephalopathy with Edema, Hypsarrhythmia and Optic atrophy) syndrome is a rare neurodegenerative disorder belonging to the group of infantile progressive encephalopathies. |
Statements
CID11:ID_976613527
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dki-india-ID_976613527
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Concluído
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15 August 2026
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