OMOP Concept 4082497
Symmetrical dyschromatosis of extremities
StandardConditionSNOMED239085000Disorder
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 Symmetrical dyschromatosis of extremities via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535729 | Dyschromatosis symmetrica hereditaria 1 | Non-standard |
| Nebraska Lexicon | 239085000 | Symmetrical dyschromatosis of extremities | Non-standard |
Synonyms
Alternative names recorded for Symmetrical dyschromatosis of extremities across source vocabularies.
- acropigmentación de Dohi
- Acropigmentation of Dohi
- discromatosis simétrica de las extremidades
- discromatosis simétrica de las extremidades (trastorno)
- Reticulate acropigmentation of Dohi
- Symmetrical dyschromatosis of extremities (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(38)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of limb
- 1Inherited cutaneous hyperpigmentation
- 2Congenital malformation
- 2Congenital pigmentary skin anomalies
- 2Developmental hereditary disorder
- 2Disorder of limb
- 2Genetic disorder of skin pigmentation
- 2Genodermatosis
- 2Hereditary disorder of the integument
- 2Hyperpigmentation of skin
- 3Congenital anomaly of skin
- 3Congenital disease
- 3Developmental disorder
- 3Disease
- 3Disorder of integument
- 3Disorder of skin pigmentation
- 3Finding of limb structure
- 3Genetic disease
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Skin deposits
- 4Clinical finding
- 4Congenital anomaly of integument
- 4Disorder of body system
- 4Disorder of fetus and/or newborn
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