OMOP Concept 4295482
Aplasia cutis in Trisomy 13 syndrome
StandardConditionSNOMED403756008Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2003
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Aplasia cutis in Trisomy 13 syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 403756008 | Aplasia cutis in Trisomy 13 syndrome | Non-standard |
Synonyms
Alternative names recorded for Aplasia cutis in Trisomy 13 syndrome across source vocabularies.
- aplasia cutánea en el síndrome de Patau
- aplasia cutánea en el síndrome de trisomía 13
- aplasia cutánea en el síndrome de trisomía 13 (trastorno)
- Aplasia cutis in Trisomy 13 syndrome (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(20)Roll up to these when you need a wider cohort.
- 1Aplasia cutis congenita
- 2Aplasia of skin
- 2Congenital anomaly of skin
- 3Congenital anomaly of integument
- 3Disorder of skin
- 4Congenital malformation
- 4Disorder involving the integument of fetus OR newborn
- 4Disorder of skin and/or subcutaneous tissue
- 4Skin finding
- 5Congenital disease
- 5Developmental disorder
- 5Disorder of fetus and/or newborn
- 5Disorder of integument
- 5Disorder of soft tissue
- 5General finding of soft tissue
- 5Integumentary system finding
- 5Skin AND/OR mucosa finding
- 6Clinical finding
- 6Disease
- 6Disorder of body system
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