OMOP Concept 608072
Generalized congenital lipodystrophy with myopathy
StandardConditionSNOMED1156814008Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2021
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Generalized congenital lipodystrophy with myopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C567642 | Lipodystrophy, Congenital Generalized, Type 4 | Non-standard |
Synonyms
Alternative names recorded for Generalized congenital lipodystrophy with myopathy across source vocabularies.
- Generalised congenital lipodystrophy type 4
- Generalised congenital lipodystrophy with myopathy
- Generalized congenital lipodystrophy type 4
- Generalized congenital lipodystrophy with myopathy (disorder)
- lipodistrofia congénita generalizada con miopatía
- lipodistrofia congénita generalizada con miopatía (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(30)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital generalized lipodystrophy
- 1Connective tissue hereditary disorder
- 1Disorder of muscle
- 1Genetic lipodystrophy
- 1Hereditary disorder of the integument
- 2Autosomal hereditary disorder
- 2Congenital connective tissue disorder
- 2Disease
- 2Disorder of connective tissue
- 2Disorder of integument
- 2Fetal and/or neonatal disorder of integument
- 2Genetic disease
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Lipodystrophy
- 2Muscle finding
- 3Clinical finding
- 3Congenital disease
- 3Degenerative disorder
- 3Disorder of body system
- 3Fetal and/or neonatal disorder
- 3Integumentary system finding
- 3Structural abnormality of adipose tissue
- 3Subcutaneous fat disorder
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