Parkinson disease LRRK2 gene mutation 12p11.23-q13.11 (Q95984): Difference between revisions
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Mutação em LRRK2 é responsável por aproximadamente 2% dos casos aparentemente esporádicos de doença de Parkinson no mundo ocidental e até 30% dos casos na população Norte Africana. É hereditário com traço autossômico dominante. | |||||||||||||||
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LRRK2 mutation is responsible for approximately 2 percent of the apparently sporadic PD in the western world and up to 30% in Northern African populations. It is inherited as a autosomal dominant trait. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/920819080 / rank | |||||||||||||||
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CID11:ID_920819080 | |||||||||||||||
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dki-india-ID_920819080 | |||||||||||||||
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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 11:49, 16 August 2026
LRRK2 mutation is responsible for approximately 2 percent of the apparently sporadic PD in the western world and up to 30% in Northern African populations. It is inherited as a autosomal dominant trait.
| Language | Label | Description | Also known as |
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| default for all languages | ID_920819080 |
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| English | Parkinson disease LRRK2 gene mutation 12p11.23-q13.11 |
LRRK2 mutation is responsible for approximately 2 percent of the apparently sporadic PD in the western world and up to 30% in Northern African populations. It is inherited as a autosomal dominant trait. |
Statements
CID11:ID_920819080
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dki-india-ID_920819080
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Concluído
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15 August 2026
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