OMOP Concept 137658
Congenital pigmentary skin anomalies
StandardConditionSNOMED205564003Disorder
Maps from
4
Descendants
62
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
4 source codes normalize to Congenital pigmentary skin anomalies via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 143776 | Congenital pigmentary skin anomalies | Non-standard |
| ICD9CM | 757.33 | Congenital pigmentary anomalies of skin | Non-standard |
| Read | PH32.00 | Congenital pigmentary skin anomalies | Non-standard |
| Read | PH32z00 | Congenital pigmentary skin anomaly NOS | Non-standard |
Synonyms
Alternative names recorded for Congenital pigmentary skin anomalies across source vocabularies.
- anomalías cutáneas pigmentarias congénitas
- anomalías cutáneas pigmentarias congénitas (trastorno)
- Congenital pigmentary anomaly of skin
- Congenital pigmentary skin anomalies (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(24)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of skin
- 1Disorder of skin pigmentation
- 2Congenital anomaly of integument
- 2Disorder of pigmentation
- 2Disorder of skin
- 2Skin lesion
- 3Congenital malformation
- 3Disease
- 3Disorder of skin and/or subcutaneous tissue
- 3Fetal and/or neonatal disorder of integument
- 3Lesion of skin and/or skin-associated mucous membrane
- 3Lesion of soft tissue
- 3Skin finding
- 4Clinical finding
- 4Congenital disease
- 4Developmental disorder
- 4Disorder of integument
- 4Disorder of soft tissue
- 4Fetal and/or neonatal disorder
- 4General finding of soft tissue
- 4Integumentary system finding
- 4Skin AND/OR mucosa finding
- 4Skin or mucosa lesion
- 5Disorder of body system
Narrower concepts
(62)Included automatically when you query with descendants.
- 1Birthmark
- 1Carney complex, trismus, pseudocamptodactyly syndrome
- 1Congenital deficiency of pigment of skin
- 1Dermal melanocytic hamartoma
- 1Familial generalized lentiginosis
- 1Familial progressive hyper and hypopigmentation
- 1Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome
- 1Inherited cutaneous hyperpigmentation
- 1McCune Albright syndrome
- 1Neuroectodermal melanolysosomal disease
- 1Pseudoleprechaunism syndrome Patterson type
- 2Acromelanosis
- 2Congenital oculocutaneous hypopigmentation
- 2Deaf blind hypopigmentation syndrome Yemenite type
- 2Deafness, vitiligo, achalasia syndrome
- 2Dermatopathia pigmentosa reticularis
- 2Dyschromatosis universalis
- 2Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome
- 2Flat birthmark
- 2Hereditary benign acanthosis nigricans
- 2Hereditary benign acanthosis nigricans with insulin resistance
- 2Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome
- 2Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies
- 2Naegeli-Franceschetti-Jadassohn syndrome
- 2Oculocerebral hypopigmentation syndrome of Preus type
Showing 25 of 62. Retrieve the full set via the API.
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