OMOP Concept 4033649
Inherited cutaneous hyperpigmentation
StandardConditionSNOMED239079007Disorder
Maps from
1
Descendants
12
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Inherited cutaneous hyperpigmentation via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 239079007 | Inherited cutaneous hyperpigmentation | Non-standard |
Synonyms
Alternative names recorded for Inherited cutaneous hyperpigmentation across source vocabularies.
- hiperpigmentación cutánea heredada
- hiperpigmentación cutánea heredada (trastorno)
- Inherited cutaneous hyperpigmentation (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(34)Roll up to these when you need a wider cohort.
- 1Congenital pigmentary skin anomalies
- 1Developmental hereditary disorder
- 1Genetic disorder of skin pigmentation
- 1Genodermatosis
- 1Hereditary disorder of the integument
- 1Hyperpigmentation of skin
- 2Congenital anomaly of skin
- 2Developmental disorder
- 2Disorder of integument
- 2Disorder of skin pigmentation
- 2Genetic disease
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Skin deposits
- 3Congenital anomaly of integument
- 3Disease
- 3Disorder of body system
- 3Disorder of pigmentation
- 3Disorder of skin
- 3Integumentary system finding
- 3Skin lesion
- 4Clinical finding
- 4Congenital malformation
- 4Disorder involving the integument of fetus OR newborn
- 4Disorder of skin and/or subcutaneous tissue
Narrower concepts
(12)Included automatically when you query with descendants.
- 1Acromelanosis
- 1Dermatopathia pigmentosa reticularis
- 1Dyschromatosis universalis
- 1Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome
- 1Hereditary benign acanthosis nigricans
- 1Hereditary benign acanthosis nigricans with insulin resistance
- 1Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome
- 1Naegeli-Franceschetti-Jadassohn syndrome
- 1Osteopathia striata, pigmentary dermopathy, white forelock syndrome
- 1Symmetrical dyschromatosis of extremities
- 1Terminal osseous dysplasia and pigmentary defect syndrome
- 1Thumb deformity, alopecia, pigmentation anomaly syndrome
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