OMOP Concept 194149
Congenital aganglionic megacolon
StandardConditionSNOMED204739008Disorder
Maps from
24
Descendants
14
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
24 source codes normalize to Congenital aganglionic megacolon via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Congenital aganglionic megacolon across source vocabularies.
- Aganglionic megacolon
- aganglionosis
- Aganglionosis
- Congenital aganglionic megacolon (disorder)
- enfermedad de Hirschsprung
- HD - Hirschsprung's disease
- Hirschsprung disease
- Hirschsprung's disease
- megacolon aganglionar
- megacolon aganglionar congénito
- megacolon aganglionar congénito (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(55)Roll up to these when you need a wider cohort.
- 1Aganglionosis of large intestine
- 1Congenital dilatation of intestinal tract
- 1Dilatation of large intestine
- 2Congenital anomaly of intestinal tract
- 2Congenital anomaly of large intestine
- 2Congenital anomaly of the peripheral nervous system
- 2Congenital malformation of autonomic nervous system
- 2Dilatation of gastrointestinal tract
- 2Dilatation of intestine
- 2Disorder of large intestine
- 2Intestinal autonomic neuropathy
- 2Motility disorder of large intestine
- 3Congenital anomaly of abdomen
- 3Congenital anomaly of digestive organ
- 3Congenital anomaly of gastrointestinal tract
- 3Congenital anomaly of lower alimentary tract
- 3Congenital anomaly of nervous system
- 3Disorder of autonomic nervous system
- 3Disorder of gastrointestinal tract
- 3Disorder of intestine
- 3Disorder of lower gastrointestinal tract
- 3Disorder of peripheral autonomic nervous system
- 3Disorder of the peripheral nervous system
- 3Finding of large intestine
- 3Motility disorder of intestine
Showing 25 of 55. Retrieve the full set via the API.
Narrower concepts
(14)Included automatically when you query with descendants.
- 1Aganglionosis of Auerbach's plexus
- 1Extensive aganglionosis Hirschsprung disease
- 1Goldberg Shprintzen megacolon syndrome
- 1Haddad syndrome
- 1Hirschsprung disease of rectosigmoid region
- 1Hirschsprung disease with deafness and polydactyly syndrome
- 1Hirschsprung disease with nail hypoplasia and dysmorphism
- 1Hirschsprung disease with type D brachydactyly syndrome
- 1Long segment Hirschsprung's disease
- 1Mowat-Wilson syndrome
- 1Short segment Hirschsprung's disease
- 1Total intestinal aganglionosis
- 1Waardenburg Shah syndrome
- 2Mowat-Wilson syndrome due to monosomy 2q22
Get this concept via the API
Resolve Congenital aganglionic megacolon - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/194149?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card