OMOP Concept 35622007
Congenital myopathy with myasthenic-like onset
StandardConditionSNOMED763315005Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2018
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Congenital myopathy with myasthenic-like onset via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 763315005 | Congenital myopathy with myasthenic-like onset | Non-standard |
Synonyms
Alternative names recorded for Congenital myopathy with myasthenic-like onset across source vocabularies.
- Congenital myopathy with myasthenic-like onset (disorder)
- miopatía congénita con comienzo similar a la miastenia
- miopatía congénita con comienzo similar a la miastenia (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(24)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of skeletal muscle
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 2Autosomal hereditary disorder
- 2Congenital anomaly of muscle AND/OR tendon
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Disorder of skeletal muscle
- 2Hereditary disease
- 2Hereditary disorder by system
- 3Congenital anomaly of musculoskeletal system
- 3Disease
- 3Disorder of body system
- 3Disorder of muscle
- 3Disorder of soft tissue
- 3Genetic disease
- 3Musculoskeletal finding
- 4Clinical finding
- 4Congenital malformation
- 4General finding of soft tissue
- 4Muscle finding
- 5Congenital disease
- 6Disorder of fetus and/or newborn
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