OMOP Concept 4034572
Dyschromatosis universalis
StandardConditionSNOMED239082002Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Dyschromatosis universalis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 141642 | Dyschromatosis universalis | Non-standard |
| Nebraska Lexicon | 239082002 | Dyschromatosis universalis | Non-standard |
Synonyms
Alternative names recorded for Dyschromatosis universalis across source vocabularies.
- discromatosis universal
- discromatosis universal (trastorno)
- Dyschromatosis universalis (disorder)
- Melanism
- melanismo
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(35)Roll up to these when you need a wider cohort.
- 1Inherited cutaneous hyperpigmentation
- 2Congenital pigmentary skin anomalies
- 2Developmental hereditary disorder
- 2Genetic disorder of skin pigmentation
- 2Genodermatosis
- 2Hereditary disorder of the integument
- 2Hyperpigmentation of skin
- 3Congenital anomaly of skin
- 3Developmental disorder
- 3Disorder of integument
- 3Disorder of skin pigmentation
- 3Genetic disease
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Skin deposits
- 4Congenital anomaly of integument
- 4Disease
- 4Disorder of body system
- 4Disorder of pigmentation
- 4Disorder of skin
- 4Integumentary system finding
- 4Skin lesion
- 5Clinical finding
- 5Congenital malformation
- 5Disorder involving the integument of fetus OR newborn
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