OMOP Concept 36717393
Aplasia cutis congenita with intestinal lymphangiectasia syndrome
StandardConditionSNOMED720500008Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Aplasia cutis congenita with intestinal lymphangiectasia syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 720500008 | Aplasia cutis congenita with intestinal lymphangiectasia syndrome | Non-standard |
Synonyms
Alternative names recorded for Aplasia cutis congenita with intestinal lymphangiectasia syndrome across source vocabularies.
- Aplasia cutis congenita with intestinal lymphangiectasia syndrome (disorder)
- Bronspiegel Zelnick syndrome
- síndrome de aplasia cutánea congénita con linfangiectasia intestinal
- síndrome de aplasia cutánea congénita con linfangiectasia intestinal (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(42)Roll up to these when you need a wider cohort.
- 1Aplasia cutis congenita
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of lower trunk
- 1Congenital anomaly of lymphatic structure of trunk
- 1Congenital lymphangiectasia
- 1Developmental hereditary disorder
- 1Hereditary disorder of lymphatic system
- 1Hereditary disorder of the integument
- 1Intestinal lymphangiectasis
- 2Aplasia of skin
- 2Autosomal hereditary disorder
- 2Congenital abnormality of lower limb and pelvic girdle
- 2Congenital anomaly of skin
- 2Congenital anomaly of trunk
- 2Developmental disorder
- 2Disorder of abdominopelvic segment of trunk
- 2Disorder of integument
- 2Disorder of lymphatic system
- 2Disorder of lymphatic vessel
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Lesion of soft tissue
- 2Lymphatic malformation
- 3Congenital anomaly of integument
- 3Congenital malformation
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