OMOP Concept 4138253
Malabsorption syndrome
StandardConditionSNOMED32230006Disorder
Maps from
7
Descendants
82
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
7 source codes normalize to Malabsorption syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| HPO | HP_0002024 | Malabsorption | Non-standard |
| MeSH | D008286 | Malabsorption Syndromes | Non-standard |
| Nebraska Lexicon | 32230006 | Malabsorption syndrome | Non-standard |
| OXMIS | 2691 | SYNDROME MALABSORPTION | Non-standard |
| Read | J69yz00 | Other gastrointestinal tract malabsorption NOS | Non-standard |
| Read | J69yz13 | Malabsorption syndrome NOS | Non-standard |
| UK Biobank | 6-1456 | malabsorption/coeliac disease | Non-standard |
Synonyms
Alternative names recorded for Malabsorption syndrome across source vocabularies.
- Malabsorption
- Malabsorption syndrome (disorder)
- síndrome de malabsorción
- síndrome de malabsorción (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(8)Roll up to these when you need a wider cohort.
Narrower concepts
(82)Included automatically when you query with descendants.
- 1Autoimmune enteropathy
- 1Bile acid malabsorption syndrome
- 1Blind loop syndrome
- 1Celiac disease
- 1Chemically-induced malabsorption
- 1Chronic steatorrhea
- 1Collagenous gastritis
- 1Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells
- 1Congenital microvillous atrophy
- 1Congenital monosaccharide malabsorption
- 1Congenital secretory diarrhea, chloride type
- 1Gastrointestinal malabsorption syndrome co-occurrent with human immunodeficiency virus infection
- 1Glucose-galactose malabsorption
- 1Intestinal disaccharidase deficiency
- 1Intestinal enteropeptidase deficiency
- 1Intestinal malabsorption
- 1Malabsorption caused by drug
- 1Malabsorption caused by infective agent
- 1Malabsorption in the elderly
- 1Malabsorption - iron
- 1Malabsorption syndrome due to acquired intolerance to fructose
- 1Malabsorption syndrome due to intolerance to lactose
- 1Neonatal malabsorption with gastrointestinal hormone-secreting endocrine tumor
- 1Non-gluten sensitive enteropathy syndrome
- 1Nonpersistence of intestinal lactase
- 1Pancreatic malabsorption
- 1Pancreatic triacylglycerol lipase deficiency
- 1Post-infective malabsorption
- 1Postprocedural steatorrhea
- 1Post-surgical malabsorption
- 1Primary malabsorption of infancy
- 1Protein-losing enteropathy
- 1Short bowel syndrome
- 1Sprue
- 1Tryptophan malabsorption syndrome
- 2Acquired short bowel syndrome
- 2Adult form of celiac disease
- 2Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome
- 2Avian malabsorption syndrome
- 2Bile acid malabsorption syndrome type I
- 2Bile acid malabsorption syndrome type II
- 2Bile acid malabsorption syndrome type III
- 2Celiac crisis
- 2Celiac disease with diffuse intestinal ulceration
- 2Celiac disease with epilepsy and cerebral calcification syndrome
- 2Complement hyperactivation, angiopathic thrombosis, protein losing enteropathy syndrome
- 2Congenital blind loop syndrome
- 2Congenital chronic diarrhea with protein-losing enteropathy
- 2Congenital short bowel syndrome
- 2Diarrhea caused by alcohol intake
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