OMOP Concept 4345481
Muscular dystrophy not predominantly limb girdle in distribution
StandardConditionSNOMED240070002Disorder
Maps from
1
Descendants
25
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Muscular dystrophy not predominantly limb girdle in distribution via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 240070002 | Muscular dystrophy not predominantly limb girdle in distribution | Non-standard |
Synonyms
Alternative names recorded for Muscular dystrophy not predominantly limb girdle in distribution across source vocabularies.
- distrofia muscular con distribución no predominante en cintura de extremidad
- distrofia muscular con distribución no predominante en cintura de extremidad (trastorno)
- Muscular dystrophy not predominantly limb girdle in distribution (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(18)Roll up to these when you need a wider cohort.
- 1Muscular dystrophy
- 2Chronic disease of musculoskeletal system
- 2Degenerative disorder of muscle
- 2Degenerative disorder of musculoskeletal system
- 2Developmental disorder
- 2Disorder of skeletal muscle
- 2Genetic disease
- 3Chronic disease
- 3Degenerative disorder
- 3Disease
- 3Disorder of muscle
- 3Disorder of musculoskeletal system
- 3Disorder of soft tissue
- 4Clinical finding
- 4Disorder of body system
- 4General finding of soft tissue
- 4Muscle finding
- 4Musculoskeletal finding
Narrower concepts
(25)Included automatically when you query with descendants.
- 1Autosomal dominant muscular dystrophy not predominantly limb girdle
- 1Autosomal recessive muscular dystrophy not predominantly limb girdle
- 1Distal muscular dystrophy
- 1X-linked muscular dystrophy not predominantly limb girdle
- 2Adenylosuccinate synthetase-like 1-related distal myopathy
- 2Adult-onset distal myopathy due to valosin containing protein mutation
- 2Benign congenital muscular dystrophy with finger flexion contractures
- 2Benign scapuloperoneal muscular dystrophy
- 2Distal anoctaminopathy
- 2Distal muscular dystrophy, Miyoshi type
- 2Distal muscular dystrophy with juvenile onset
- 2Distal myopathy 2
- 2Distal myopathy Welander type
- 2Distal myopathy with anterior tibial onset
- 2Distal myopathy with posterior leg and anterior hand involvement
- 2Distal nebulin myopathy
- 2Facioscapulohumeral muscular dystrophy
- 2Finnish upper limb onset distal myopathy
- 2KLHL9-related early-onset distal myopathy
- 2Laing early-onset distal myopathy
- 2Oculopharyngeal muscular dystrophy
- 2Oculopharyngodistal myopathy
- 2Progressive scapulohumeroperoneal distal myopathy
- 2Scapulohumeral muscular dystrophy
- 2Tibial muscular dystrophy
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