Single seizure due to genetic syndromes with widespread or progressive effects (Q83756): Difference between revisions
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Convulsão não provocada ocorrendo em paciente com uma condição geneticamente determinada em que a epilepsia coexiste com incapacidade intelectual e/ou características dismórficas. Inclui crises epilépticas devidas a anormalidades autossômicas, ligadas ao X, mitocondriais ou cromossômicas. | |||||||||||||||
| description / en | description / en | ||||||||||||||
An unprovoked seizure occurring in a patient with a genetically determined condition in which epilepsy coexists with mental retardation and/or dysmorphic features. Includes seizures due to autosomal, X-linked, mitochondrial or chromosomal abnormalities. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/734748791 / rank | |||||||||||||||
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CID11:ID_734748791 | |||||||||||||||
| Property / CURIE: CID11:ID_734748791 / rank | |||||||||||||||
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dki-india-ID_734748791 | |||||||||||||||
| Property / Canary Token: dki-india-ID_734748791 / rank | |||||||||||||||
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Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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Latest revision as of 09:07, 15 August 2026
An unprovoked seizure occurring in a patient with a genetically determined condition in which epilepsy coexists with mental retardation and/or dysmorphic features. Includes seizures due to autosomal, X-linked, mitochondrial or chromosomal abnormalities.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_734748791 |
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| English | Single seizure due to genetic syndromes with widespread or progressive effects |
An unprovoked seizure occurring in a patient with a genetically determined condition in which epilepsy coexists with mental retardation and/or dysmorphic features. Includes seizures due to autosomal, X-linked, mitochondrial or chromosomal abnormalities. |
Statements
CID11:ID_734748791
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dki-india-ID_734748791
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Concluído
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13 August 2026
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