OMOP Concept 45771254
CHMP2B-related frontotemporal dementia
StandardConditionSNOMED702393003Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2014
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to CHMP2B-related frontotemporal dementia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C579991 | Chromosome 3-Linked Frontotemporal Dementia | Non-standard |
| Nebraska Lexicon | 702393003 | Frontotemporal dementia with gene located on 3p11 | Non-standard |
Synonyms
Alternative names recorded for CHMP2B-related frontotemporal dementia across source vocabularies.
- Chromosome 3-linked frontotemporal dementia
- demencia frontotemporal asociada con la proteína CHMP2B
- demencia frontotemporal asociada con mutación genética en 3p11
- demencia frontotemporal asociada con mutación genética en 3p11 (trastorno)
- Frontotemporal dementia with gene located on 3p11
- Frontotemporal dementia with gene located on 3p11 (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(30)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Frontotemporal dementia
- 1Hereditary degenerative disease of central nervous system
- 2Autosomal hereditary disorder
- 2Degenerative disease of the central nervous system
- 2Dementia
- 2Frontotemporal degeneration
- 2Hereditary disorder of nervous system
- 3Cerebral degeneration
- 3Degenerative disorder
- 3Disorder of nervous system
- 3Disorder of the central nervous system
- 3Finding of head region
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Impaired cognition
- 3Organic mental disorder
- 4Central nervous system finding
- 4Cognitive function finding
- 4Degenerative brain disorder
- 4Disease
- 4Disorder of body system
- 4Disorder of brain
- 4Genetic disease
- 4Head finding
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