OMOP Concept 4297463
Oculopharyngeal muscular dystrophy
StandardConditionSNOMED77097004Disorder
Maps from
7
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
7 source codes normalize to Oculopharyngeal muscular dystrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 115004 | Oculopharyngeal muscular dystrophy | Non-standard |
| CIEL | 115005 | Shy-Gonatas Syndrome | Non-standard |
| CIEL | 115011 | Kiloh-Nevin syndrome | Non-standard |
| MeSH | D039141 | Muscular Dystrophy, Oculopharyngeal | Non-standard |
| Nebraska Lexicon | 77097004 | Oculopharyngeal muscular dystrophy | Non-standard |
| Read | F391600 | Ocular muscular dystrophy | Non-standard |
| Read | F391700 | Oculopharyngeal muscular dystrophy | Non-standard |
Synonyms
Alternative names recorded for Oculopharyngeal muscular dystrophy across source vocabularies.
- distrofia muscular oculofaríngea
- distrofia muscular oculofaríngea (trastorno)
- distrofia oculofaríngea
- Oculopharyngeal dystrophy
- Oculopharyngeal muscular dystrophy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(86)Roll up to these when you need a wider cohort.
- 1Autosomal dominant muscular dystrophy not predominantly limb girdle
- 1Chronic digestive system disorder
- 1Chronic disease of ocular adnexa
- 1Chronic disease of respiratory system
- 1Congenital anomaly of neck
- 1Congenital anomaly of ocular adnexa
- 1Congenital anomaly of pharynx
- 1Congenital structural abnormality of orbit
- 1Digestive system hereditary disorder
- 1Hereditary disorder of the visual system
- 1Musculoskeletal disorder of the neck
- 1Myopathy of extraocular muscles
- 2Autosomal dominant hereditary disorder
- 2Chronic disease
- 2Congenital anomaly of digestive organ
- 2Congenital anomaly of head
- 2Congenital anomaly of upper respiratory system
- 2Congenital anomaly of visual system
- 2Congenital hereditary muscular dystrophy
- 2Congenital malformation
- 2Congenital malformation of upper alimentary tract
- 2Disorder of digestive system
- 2Disorder of extraocular muscle
- 2Disorder of musculoskeletal system
- 2Disorder of neck
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