OMOP Concept 4033871
Familial pigmented purpuric eruption
StandardConditionSNOMED238783008Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Familial pigmented purpuric eruption via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537186 | Pigmented purpuric eruption | Non-standard |
| Nebraska Lexicon | 238783008 | Familial pigmented purpuric eruption | Non-standard |
Synonyms
Alternative names recorded for Familial pigmented purpuric eruption across source vocabularies.
- erupción purpúrica pigmentada familiar
- erupción purpúrica pigmentada familiar (trastorno)
- Familial capillaritis
- Familial pigmented purpuric eruption (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(51)Roll up to these when you need a wider cohort.
- 1Familial disease
- 1Pigmented purpuric dermatosis
- 2Capillaritis
- 2Chronic disease of cardiovascular system
- 2Chronic disease of skin
- 2Disease
- 2Hemosiderin pigmentation of skin
- 2Papular eruption
- 2Purpuric disorder
- 2Purpuric rash
- 2Vasculitis of the skin
- 3Bleeding skin
- 3Chronic disease
- 3Clinical finding
- 3Disorder of capillaries
- 3Disorder of cardiovascular system
- 3Disorder of hemostatic system
- 3Disorder of skin
- 3Disorder of skin pigmentation
- 3Eruption
- 3Inflammatory dermatosis
- 3Papule of skin
- 3Skin deposits
- 3Skin lesion
- 3Vascular disease of the skin
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