OMOP Concept 37397476
Piebaldism
StandardConditionSNOMED718122005Disorder
Maps from
6
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
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Source codes that map to this concept
6 source codes normalize to Piebaldism via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 158362 | Piebaldism | Non-standard |
| HPO | HP_0007544 | Piebald skin depigmentation | Non-standard |
| MeSH | D016116 | Piebaldism | Non-standard |
| Nebraska Lexicon | 718122005 | Piebaldism | Non-standard |
| Nebraska Lexicon | 79417003 | Autosomal dominant oculocutaneous albinism | Non-standard |
| Read | C302A11 | Piebaldism | Non-standard |
Synonyms
Alternative names recorded for Piebaldism across source vocabularies.
- Piebaldism (disorder)
- piebaldismo
- piebaldismo (trastorno)
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.
- 1Autosomal dominant hereditary disorder
- 1Congenital deficiency of pigment of skin
- 1Developmental hereditary disorder
- 1Genetic disorder of skin pigmentation
- 1Hereditary disorder of the integument
- 2Autosomal hereditary disorder
- 2Congenital pigmentary skin anomalies
- 2Developmental disorder
- 2Disorder of integument
- 2Disorder of skin pigmentation
- 2Genetic disease
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Skin hypopigmented
- 3Congenital anomaly of skin
- 3Disease
- 3Disorder of body system
- 3Disorder of pigmentation
- 3Integumentary system finding
- 3Skin lesion
- 4Clinical finding
- 4Congenital anomaly of integument
- 4Disorder of skin
- 4Lesion of skin and/or skin-associated mucous membrane
- 4Lesion of soft tissue
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