OMOP Concept 36716157
Oculogastrointestinal muscular dystrophy
StandardConditionSNOMED722060007Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Oculogastrointestinal muscular dystrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536350 | Visceral myopathy familial external ophthalmoplegia | Non-standard |
| Nebraska Lexicon | 722060007 | Visceral myopathy with familial external ophthalmoplegia syndrome | Non-standard |
Synonyms
Alternative names recorded for Oculogastrointestinal muscular dystrophy across source vocabularies.
- distrofia muscular oculogastrointestinal
- distrofia muscular oculogastrointestinal (trastorno)
- Oculogastrointestinal muscular dystrophy (disorder)
- Visceral myopathy with familial external ophthalmoplegia syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(48)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of intestinal tract
- 1Congenital anomaly of visual system
- 1Developmental hereditary disorder
- 1Digestive system hereditary disorder
- 1Hereditary disorder of the visual system
- 1Pseudo-obstruction of intestine
- 2Autosomal hereditary disorder
- 2Congenital anomaly of abdomen
- 2Congenital anomaly of digestive organ
- 2Congenital anomaly of gastrointestinal tract
- 2Congenital malformation
- 2Developmental disorder
- 2Disorder of digestive system
- 2Disorder of intestine
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Motility disorder of intestine
- 2Pseudo-obstruction of gastrointestinal tract
- 2Visual system disorder
- 3Bowel finding
- 3Congenital anomaly of digestive system
- 3Congenital anomaly of digestive tract
- 3Congenital anomaly of lower trunk
- 3Congenital disease
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