OMOP Concept 45765480
Frontotemporal dementia with parkinsonism-17
StandardConditionSNOMED702429008Disorder
Maps from
1
Descendants
1
Valid from
31 Jul 2014
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Frontotemporal dementia with parkinsonism-17 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 702429008 | Disinhibition-dementia-parkinsonism-amytrophy complex | Non-standard |
Synonyms
Alternative names recorded for Frontotemporal dementia with parkinsonism-17 across source vocabularies.
- complejo de desinhibición-demencia-parkinsonismo-amiotrofia
- demencia frontotemporal asociada con parkinsonismo ligado al cromosoma 17
- demencia frontotemporal asociada con parkinsonismo ligado al cromosoma 17 (trastorno)
- Disinhibition-dementia-parkinsonism-amytrophy complex
- enfermedad de Pick familiar
- enfermedad de Wilhelmsen-Lynch
- Familial Pick's disease
- Frontotemporal dementia with parkinsonism-17 (disorder)
- FTDP-17 - Frontotemporal dementia with parkinsonism 17
- Wilhelmsen-Lynch disease
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(18)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Disorder of brain
- 1Hereditary disorder of nervous system
- 1Movement disorder
- 2Autosomal hereditary disorder
- 2Disease
- 2Disorder of head
- 2Disorder of nervous system
- 2Disorder of the central nervous system
- 2Finding of brain
- 2Finding of movement
- 2Hereditary disorder by system
- 3Central nervous system finding
- 3Clinical finding
- 3Disorder of body system
- 3Head finding
- 3Hereditary disease
- 4Genetic disease
Narrower concepts
(1)Included automatically when you query with descendants.
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