OMOP Concept 36715518
Hirschsprung disease with type D brachydactyly syndrome
StandardConditionSNOMED721222007Disorder
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 Hirschsprung disease with type D brachydactyly syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 721222007 | Hirschsprung disease with type D brachydactyly syndrome | Non-standard |
Synonyms
Alternative names recorded for Hirschsprung disease with type D brachydactyly syndrome across source vocabularies.
- Hirschsprung disease with type D brachydactyly syndrome (disorder)
- síndrome de enfermedad de Hirschsprung con braquidactilia tipo D
- síndrome de enfermedad de Hirschsprung con braquidactilia tipo D (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(81)Roll up to these when you need a wider cohort.
- 1Brachydactyly
- 1Congenital aganglionic megacolon
- 1Congenital dilatation of colon
- 1Developmental hereditary disorder
- 1Digestive system hereditary disorder
- 1Inherited autonomic nervous system disorder
- 1Multiple malformation syndrome with limb defect as major feature
- 2Aganglionosis of large intestine
- 2Congenital abnormal shape of digit
- 2Congenital anomaly of large intestine
- 2Congenital anomaly of the peripheral nervous system
- 2Congenital dilatation of intestinal tract
- 2Developmental disorder
- 2Dilatation of large intestine
- 2Disorder of autonomic nervous system
- 2Disorder of colon
- 2Disorder of digestive system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Hereditary disorder of nervous system
- 2Longitudinal deficiency of part of limb
- 2Motility disorder of large intestine
- 2Multiple system malformation syndrome
- 3Congenital anomaly of digit
- 3Congenital anomaly of intestinal tract
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