OMOP Concept 194149
Congenital aganglionic megacolon
StandardConditionSNOMED204739008Disorder
Maps from
26
Descendants
14
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
26 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
(56)Roll up to these when you need a wider cohort.
- 1Aganglionosis of large intestine
- 1Congenital anomaly of the peripheral nervous system
- 1Congenital dilatation of intestinal tract
- 1Dilatation of large intestine
- 1Motility disorder of large intestine
- 2Congenital anomaly of intestinal tract
- 2Congenital anomaly of large intestine
- 2Congenital anomaly of nervous system
- 2Congenital malformation of autonomic nervous system
- 2Dilatation of intestine
- 2Disorder of large intestine
- 2Disorder of the peripheral nervous system
- 2Intestinal autonomic neuropathy
- 2Motility disorder of intestine
- 3Autonomic neuropathy
- 3Congenital anomaly of abdomen
- 3Congenital anomaly of digestive organ
- 3Congenital anomaly of gastrointestinal tract
- 3Congenital anomaly of lower alimentary tract
- 3Congenital malformation
- 3Dilatation of gastrointestinal tract
- 3Disorder of autonomic nervous system
- 3Disorder of intestine
- 3Disorder of lower gastrointestinal tract
- 3Disorder of nervous system
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
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