OMOP Concept 4027537
Neuromuscular junction disorder
StandardConditionSNOMED128213006Disorder
Maps from
5
Descendants
54
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
5 source codes normalize to Neuromuscular junction disorder via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 133088 | Neuromuscular junction disorder | Non-standard |
| MeSH | D020511 | Neuromuscular Junction Diseases | Non-standard |
| Read | F38y.00 | Other specific myoneural disorder | Non-standard |
| Read | F38z.00 | Myoneural disorder NOS | Non-standard |
| Read | Fyu8.00 | [X]Diseases of myoneural junction and muscle | Non-standard |
Synonyms
Alternative names recorded for Neuromuscular junction disorder across source vocabularies.
- Neuromuscular junction disorder (disorder)
- trastorno de la unión neuromuscular
- trastorno de la unión neuromuscular (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(6)Roll up to these when you need a wider cohort.
Narrower concepts
(54)Included automatically when you query with descendants.
- 1Acquired neuromuscular ptosis
- 1Disorder of neuromuscular transmission
- 1Generalized hypotonia due to neuromuscular junction defect
- 1Hereditary motor end-plate disease
- 1Neuromuscular junction disorder due to Lambert-Eaton syndrome
- 1Toxic neuromuscular junction disorder
- 2Amyotonia congenita
- 2Cholinergic crisis
- 2Disorder of neuromuscular junction caused by botulinum toxin
- 2Drug-induced myasthenia
- 2Eaton-Lambert syndrome
- 2Myasthenia gravis
- 2Myasthenia gravis caused by MuSK (muscle-specific kinase) antibodies
- 2Myasthenic syndrome due to another disorder
- 2Myopathy in myasthenia gravis
- 2Neuromuscular junction disorder due to ingestion of organic phosphorus compound
- 2Pelagic paralysis
- 2Slow channel syndrome
- 2Tick paralysis
- 3Antibiotic-induced neuromuscular blocking
- 3Congenital myasthenic syndrome with glycosylation defect due to ALG14 UDP-N-acetylglucosaminyltransferase subunit gene mutation
- 3Eaton Lambert syndrome without underlying malignancy
- 3Eaton Lambert syndrome with underlying malignancy
- 3Exacerbation of myasthenia gravis
- 3Generalized myasthenia
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