OMOP Concept 4244026
Congenital dilatation of intestinal tract
StandardConditionSNOMED93058003Disorder
Maps from
1
Descendants
19
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Congenital dilatation of intestinal tract via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 93058003 | Congenital dilatation of intestinal tract | Non-standard |
Synonyms
Alternative names recorded for Congenital dilatation of intestinal tract across source vocabularies.
- Congenital dilatation of intestinal tract (disorder)
- Congenital enlarged intestine
- Congenital enteromegaly
- dilatación congénita del tracto intestinal
- dilatación congénita del tracto intestinal (trastorno)
- enteromegalia congénita
- intestino agrandado congénito
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.
- 1Congenital anomaly of intestinal tract
- 1Dilatation of intestine
- 2Congenital anomaly of abdomen
- 2Congenital anomaly of digestive organ
- 2Congenital anomaly of gastrointestinal tract
- 2Dilatation of gastrointestinal tract
- 2Disorder of intestine
- 3Bowel finding
- 3Congenital anomaly of digestive system
- 3Congenital anomaly of digestive tract
- 3Congenital anomaly of lower trunk
- 3Disorder of abdomen
- 3Disorder of digestive organ
- 3Disorder of gastrointestinal tract
- 4Abdominal organ finding
- 4Congenital abnormality of lower limb and pelvic girdle
- 4Congenital anomaly of trunk
- 4Congenital malformation
- 4Disorder of abdominopelvic segment of trunk
- 4Disorder of digestive system
- 4Disorder of digestive system specific to fetus OR newborn
- 4Disorder of digestive tract
- 4Finding of abdomen
- 4Gastrointestinal tract finding
- 5Congenital disease
Narrower concepts
(19)Included automatically when you query with descendants.
- 1Congenital aganglionic megacolon
- 1Congenital dilatation of colon
- 1Congenital megaduodenum
- 1Hirschsprung disease, ganglioneuroblastoma syndrome
- 2Aganglionosis of Auerbach's plexus
- 2Extensive aganglionosis Hirschsprung disease
- 2Goldberg Shprintzen megacolon syndrome
- 2Haddad syndrome
- 2Hirschsprung disease of rectosigmoid region
- 2Hirschsprung disease with deafness and polydactyly syndrome
- 2Hirschsprung disease with nail hypoplasia and dysmorphism
- 2Hirschsprung disease with type D brachydactyly syndrome
- 2Long segment Hirschsprung's disease
- 2Mowat-Wilson syndrome
- 2Secondary megacolon - congenital
- 2Short segment Hirschsprung's disease
- 2Total intestinal aganglionosis
- 2Waardenburg Shah syndrome
- 3Mowat-Wilson syndrome due to monosomy 2q22
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