OMOP Concept 4031808
Disorder of lipid storage and metabolism
StandardConditionSNOMED238017009Disorder
Maps from
8
Descendants
92
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
8 source codes normalize to Disorder of lipid storage and metabolism via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 117964 | Familial Splenic Anemia | Non-standard |
| CIEL | 142055 | Disorder of Lipid Storage and Metabolism | Non-standard |
| CIM10 | E75 | Disorders of sphingolipid metabolism and other lipid storage disorders | Non-standard |
| ICD10 | E75 | Disorders of sphingolipid metabolism and other lipid storage disorders | Non-standard |
| ICD10CM | E75 | Disorders of sphingolipid metabolism and other lipid storage disorders | Non-standard |
| ICD10CN | E75 | Disorders of sphingolipid metabolism and other lipid storage disorders | Non-standard |
| ICD10GM | E75 | Disorders of sphingolipid metabolism and other lipid storage disorders | Non-standard |
| KCD7 | E75 | Disorders of sphingolipid metabolism and other lipid storage disorders | Non-standard |
Synonyms
Alternative names recorded for Disorder of lipid storage and metabolism across source vocabularies.
- Disorder of lipid storage and metabolism (disorder)
- trastorno del metabolismo y depósito de lípidos
- trastorno del metabolismo y depósito de lípidos (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
Narrower concepts
(92)Included automatically when you query with descendants.
- 1Abnormal lipid deposits
- 1Disorder of cholesterol catabolism
- 1Disorder of cholesterol synthesis
- 1Farber's lipogranulomatosis
- 1Gangliosidosis
- 1GM3 synthase deficiency
- 1Lipid storage disease
- 1Lipoidosis
- 1Lysosomal acid lipase deficiency
- 1Pancreatic triacylglycerol lipase deficiency
- 1Sjögren-Larsson syndrome
- 1Sphingolipidosis
- 23-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency
- 2Autosomal recessive cerebellar ataxia with late-onset spasticity
- 2Cerebral lipidosis
- 2Chemically-induced lipidosis
- 2Cholestanol storage disease
- 2Cholesterol ester storage disease
- 2Chondrodysplasia punctata, X-linked dominant type
- 2Delta-4-3-oxosteroid-5-beta-reductase deficiency
- 2Desmosterolosis
- 2Encephalopathy due to prosaposin deficiency
- 2Fabry's disease
- 2Galactosylceramide beta-galactosidase deficiency
- 2Gaucher's disease
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