OMOP Concept 36717214
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells
StandardConditionSNOMED722392003Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563673 | Diarrhea 4, Malabsorptive, Congenital | Non-standard |
Synonyms
Alternative names recorded for Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells across source vocabularies.
- anendocrinosis entérica
- Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder)
- Congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells
- diarrea congénita con mala absorción debida a escasez de células enteroendocrinas
- diarrea congénita con mala absorción debida a escasez de células enteroendocrinas (trastorno)
- Enteric anendocrinosis
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(34)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Chronic diarrhea of infants AND/OR young children
- 1Congenital disease
- 1Digestive system hereditary disorder
- 1Disorder of digestive system specific to fetus OR newborn
- 1Malabsorption syndrome
- 2Autosomal hereditary disorder
- 2Chronic diarrhea
- 2Disorder of digestive system
- 2Disorder of gastrointestinal tract
- 2Fetal and/or neonatal disorder
- 2Hereditary disorder by system
- 3Chronic digestive system disorder
- 3Diarrhea
- 3Digestive system finding
- 3Disease
- 3Disorder of body system
- 3Disorder of digestive tract
- 3Disorder of intestine
- 3Gastrointestinal tract finding
- 3Hereditary disease
- 4Bowel finding
- 4Chronic disease
- 4Clinical finding
- 4Disorder of abdomen
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