OMOP Concept 44783251
Neutral lipid storage disease with myopathy
StandardConditionSNOMED699315005Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2014
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Neutral lipid storage disease with myopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C565192 | Neutral Lipid Storage Disease with Myopathy | Non-standard |
Synonyms
Alternative names recorded for Neutral lipid storage disease with myopathy across source vocabularies.
- enfermedad de almacenamiento de lípidos neutros con miopatía
- enfermedad de almacenamiento de lípidos neutros con miopatía (trastorno)
- enfermedad de almacenamiento de lípidos neutros sin ictiosis
- Neutral lipid storage disease with myopathy (disorder)
- Neutral lipid storage disease without ichthyosis
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(28)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Lipid storage myopathy
- 2Autosomal hereditary disorder
- 2Hereditary disorder of musculoskeletal system
- 2Lipid storage disease
- 2Metabolic myopathy
- 3Disorder of lipid storage and metabolism
- 3Disorder of lysosomal enzyme
- 3Disorder of musculoskeletal system
- 3Disorder of skeletal muscle
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Inborn error of metabolism
- 4Congenital disease
- 4Disorder of body system
- 4Disorder of lipoprotein AND/OR lipid metabolism
- 4Disorder of muscle
- 4Disorder of soft tissue
- 4Enzymopathy
- 4Genetic disease
- 4Hereditary metabolic disease
- 4Musculoskeletal finding
- 5Clinical finding
- 5Disease
- 5Fetal and/or neonatal disorder
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