OMOP Concept 35622370
Oculopharyngodistal myopathy
StandardConditionSNOMED763829004Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2018
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Oculopharyngodistal myopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563508 | Oculopharyngodistal Myopathy | Non-standard |
| Nebraska Lexicon | 763829004 | OPDM - oculopharyngodistal myopathy | Non-standard |
Synonyms
Alternative names recorded for Oculopharyngodistal myopathy across source vocabularies.
- miopatía oculofaringodistal
- miopatía oculofaringodistal (trastorno)
- Oculopharyngeal distal myopathy
- Oculopharyngodistal myopathy (disorder)
- OPDM - oculopharyngodistal myopathy
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(67)Roll up to these when you need a wider cohort.
- 1Chronic digestive system disorder
- 1Chronic disease of ocular adnexa
- 1Chronic disease of respiratory system
- 1Digestive system hereditary disorder
- 1Disorder of pharynx
- 1Distal muscular dystrophy
- 1Hereditary disorder of the visual system
- 1Musculoskeletal disorder of the neck
- 1Pharyngeal paresis
- 1Ptosis of eyelid
- 2Autosomal hereditary disorder
- 2Chronic disease
- 2Disorder of digestive organ
- 2Disorder of digestive system
- 2Disorder of eyelid
- 2Disorder of musculoskeletal system
- 2Disorder of neck
- 2Disorder of ocular adnexa
- 2Disorder of respiratory system
- 2Disorder of upper digestive tract
- 2Disorder of upper respiratory system
- 2Finding of neck region
- 2Finding of pharynx
- 2Hereditary disorder by system
- 2Hereditary progressive muscular dystrophy
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