Familial Parkinson disease (Q41060): Difference between revisions
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Subtipo familiar da doença de Parkinson, um transtorno causado pela degeneração neuronal dopaminérgica progressiva da substância negra, que se caracteriza por tremor de repouso, bradicinesia e rigidez. Os casos familiares podem ser causados por mutações nos genes LRRK2, PARK7, PINK1, PRKN ou SNCA. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Familial subtype of Parkinson Disease, a disorder caused by progressive dopaminergic neuron degeneration of the substantia nigra that is characterized by resting tremor, bradykinesia, and rigidity. Familial cases can be caused by mutations in LRRK2, PARK7, PINK1, PRKN, or SNCA genes. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/811427861 / rank | |||||||||||||||
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CID11:8A00.01 | |||||||||||||||
| Property / CURIE: CID11:8A00.01 / rank | |||||||||||||||
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dki-india-8A00.01 | |||||||||||||||
| Property / Canary Token: dki-india-8A00.01 / rank | |||||||||||||||
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Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
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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 / Collection date: 13 August 2026 / rank | |||||||||||||||
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| Property / Linked ICD 10: G20 / rank | |||||||||||||||
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Latest revision as of 07:07, 13 August 2026
Familial subtype of Parkinson Disease, a disorder caused by progressive dopaminergic neuron degeneration of the substantia nigra that is characterized by resting tremor, bradykinesia, and rigidity. Familial cases can be caused by mutations in LRRK2, PARK7, PINK1, PRKN, or SNCA genes.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A00.01 |
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| English | Familial Parkinson disease |
Familial subtype of Parkinson Disease, a disorder caused by progressive dopaminergic neuron degeneration of the substantia nigra that is characterized by resting tremor, bradykinesia, and rigidity. Familial cases can be caused by mutations in LRRK2, PARK7, PINK1, PRKN, or SNCA genes. |
Statements
CID11:8A00.01
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dki-india-8A00.01
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Concluído
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13 August 2026
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