OMOP Concept 4003983
Hereditary benign acanthosis nigricans
StandardConditionSNOMED205583005Disorder
Maps from
1
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
1 source code normalizes to Hereditary benign acanthosis nigricans via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Read | PH3y500 | Acanthosis nigricans, congenital | Non-standard |
Synonyms
Alternative names recorded for Hereditary benign acanthosis nigricans across source vocabularies.
- acantosis nigricans benigna hereditaria
- acantosis nigricans benigna hereditaria (trastorno)
- Hereditary benign acanthosis nigricans (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(43)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Benign acanthosis nigricans
- 1Congenital melanosis
- 1Hereditary hypermelanosis
- 1Inherited cutaneous hyperpigmentation
- 2Autosomal hereditary disorder
- 2Congenital disease
- 2Congenital pigmentary skin anomalies
- 2Developmental hereditary disorder
- 2Genetic disorder of skin pigmentation
- 2Genodermatosis
- 2Hereditary disorder of the integument
- 2Hyperpigmentation of skin
- 2Keratoderma
- 2Melanosis
- 3Congenital anomaly of skin
- 3Developmental disorder
- 3Disorder of integument
- 3Disorder of pigmentation
- 3Disorder of skin
- 3Disorder of skin pigmentation
- 3Fetal and/or neonatal disorder
- 3Genetic disease
- 3Hereditary disease
- 3Hereditary disorder by system
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