OMOP Concept 4344042
Muscular dystrophy with predominantly proximal limb girdle distribution
StandardConditionSNOMED240046001Disorder
Maps from
8
Descendants
51
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
8 source codes normalize to Muscular dystrophy with predominantly proximal limb girdle distribution via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 116302 | Limb-girdle muscular dystrophy | Non-standard |
| HPO | HP_0006785 | Limb-girdle muscular dystrophy | Non-standard |
| ICD10CM | G71.03 | Limb girdle muscular dystrophies | Non-standard |
| ICD10CM | G71.038 | Other limb girdle muscular dystrophy | Non-standard |
| MeSH | D049288 | Muscular Dystrophies, Limb-Girdle | Non-standard |
| Read | F391100 | Erb's muscular dystrophy | Non-standard |
| Read | F391200 | Pelvic muscular dystrophy | Non-standard |
| Read | F391300 | Other limb-girdle muscular dystrophy | Non-standard |
Synonyms
Alternative names recorded for Muscular dystrophy with predominantly proximal limb girdle distribution across source vocabularies.
- distrofia muscular con distribución predominante en cinturas proximales de extremidades
- distrofia muscular con distribución predominante en cinturas proximales de extremidades (trastorno)
- Limb-girdle muscular dystrophy
- Muscular dystrophy with predominantly proximal limb girdle distribution (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(23)Roll up to these when you need a wider cohort.
- 1Hereditary progressive muscular dystrophy
- 2Developmental hereditary disorder
- 2Hereditary disorder of musculoskeletal system
- 2Muscular dystrophy
- 3Chronic disease of musculoskeletal system
- 3Degenerative disorder of muscle
- 3Degenerative disorder of musculoskeletal system
- 3Developmental disorder
- 3Disorder of musculoskeletal system
- 3Disorder of skeletal muscle
- 3Genetic disease
- 3Hereditary disease
- 3Hereditary disorder by system
- 4Chronic disease
- 4Degenerative disorder
- 4Disease
- 4Disorder of body system
- 4Disorder of muscle
- 4Disorder of soft tissue
- 4Musculoskeletal finding
- 5Clinical finding
- 5General finding of soft tissue
- 5Muscle finding
Narrower concepts
(51)Included automatically when you query with descendants.
- 1Autosomal dominant muscular dystrophy with limb girdle distribution
- 1Autosomal recessive muscular dystrophy with limb girdle distribution
- 1X-linked muscular dystrophy with limb girdle distribution
- 2Adult onset autosomal recessive muscular dystrophy with normal dystrophin
- 2Autosomal dominant limb girdle muscular dystrophy type 1D
- 2Autosomal dominant limb girdle muscular dystrophy type 1E
- 2Autosomal dominant limb girdle muscular dystrophy type 1F
- 2Autosomal dominant limb girdle muscular dystrophy type 1G
- 2Autosomal dominant limb-girdle muscular dystrophy type 1H
- 2Autosomal dominant muscular dystrophy with gene located at 5q31
- 2Autosomal recessive limb girdle muscular dystrophy type 2A
- 2Autosomal recessive limb girdle muscular dystrophy type 2B
- 2Autosomal recessive limb girdle muscular dystrophy type 2C
- 2Autosomal recessive limb girdle muscular dystrophy type 2D
- 2Autosomal recessive limb girdle muscular dystrophy type 2E
- 2Autosomal recessive limb girdle muscular dystrophy type 2F
- 2Autosomal recessive limb girdle muscular dystrophy type 2G
- 2Autosomal recessive limb girdle muscular dystrophy type 2I
- 2Autosomal recessive limb girdle muscular dystrophy type 2J
- 2Autosomal recessive limb girdle muscular dystrophy type 2K
- 2Autosomal recessive limb girdle muscular dystrophy type 2L
- 2Autosomal recessive limb girdle muscular dystrophy type 2M
- 2Autosomal recessive limb girdle muscular dystrophy type 2N
- 2Autosomal recessive limb girdle muscular dystrophy type 2O
- 2Autosomal recessive limb girdle muscular dystrophy type 2P
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