OMOP Concept 37162672
Childhood-onset nemaline myopathy
StandardConditionSNOMED1197154006Disorder
Maps from
1
Descendants
0
Valid from
28 Feb 2022
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Childhood-onset nemaline myopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 133429 | Childhood onset nemaline myopathy | Non-standard |
Synonyms
Alternative names recorded for Childhood-onset nemaline myopathy across source vocabularies.
- Childhood-onset nemaline myopathy (disorder)
- Mild nemaline myopathy
- miopatía nemalínica de inicio en la infancia
- miopatía nemalínica de inicio en la infancia (trastorno)
- miopatía nemalínica leve
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(22)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Chronic disease of musculoskeletal system
- 1Hereditary disorder of musculoskeletal system
- 1Nemaline myopathy
- 1Progressive weakness of muscle
- 2Autosomal hereditary disorder
- 2Chronic disease
- 2Disorder of musculoskeletal system
- 2Disorder of skeletal muscle
- 2Genetic disease
- 2Hereditary disorder by system
- 2Muscle weakness
- 3Disease
- 3Disorder of body system
- 3Disorder of muscle
- 3Disorder of soft tissue
- 3Finding of power of skeletal muscle
- 3Hereditary disease
- 3Musculoskeletal finding
- 4Clinical finding
- 4General finding of soft tissue
- 4Muscle finding
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