OMOP Concept 4048654
Familial infantile myasthenia
StandardConditionSNOMED230670003Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Familial infantile myasthenia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535759 | Congenital myasthenic syndrome with episodic apnea | Non-standard |
Synonyms
Alternative names recorded for Familial infantile myasthenia across source vocabularies.
- Familial infantile myasthenia (disorder)
- FIM - Familial infantile myasthenia
- miastenia familiar infantil
- miastenia familiar infantil (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(34)Roll up to these when you need a wider cohort.
- 1Congenital myasthenic syndrome
- 1Myasthenia gravis, juvenile form
- 2Congenital disease
- 2Genetically determined myasthenia
- 2Myasthenia gravis
- 3Antibody-mediated activation and inactivation
- 3Autoimmune disease
- 3Disorder of neuromuscular transmission
- 3Fetal and/or neonatal disorder
- 3Hereditary disorder of immune system
- 3Hereditary disorder of musculoskeletal system
- 3Hereditary disorder of nervous system
- 3Immune-mediated neuropathy
- 3Myoneural disorder
- 4Disease
- 4Disorder of immune function
- 4Disorder of musculoskeletal system
- 4Disorder of nervous system
- 4Disorder of skeletal muscle
- 4Disorder of the peripheral nervous system
- 4Hereditary disorder by system
- 4Immune hypersensitivity disorder by mechanism
- 4Neuromuscular junction disorder
- 4Neuropathy
- 5Clinical finding
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