OMOP Concept 4247802
Muscular dystrophy
StandardConditionSNOMED73297009Disorder
Maps from
32
Descendants
126
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
32 source codes normalize to Muscular dystrophy via the OMOP "Maps to" relationship.
Showing 25 of 32 source codes. Retrieve the full set via the API.
Synonyms
Alternative names recorded for Muscular dystrophy across source vocabularies.
- distrofia muscular
- distrofia muscular (trastorno)
- MD - Muscular dystrophy
- Muscular dystrophy (disorder)
- PMD - Progressive muscular dystrophy
- Progressive muscular dystrophy
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(17)Roll up to these when you need a wider cohort.
- 1Chronic disease of musculoskeletal system
- 1Degenerative disorder of muscle
- 1Degenerative disorder of musculoskeletal system
- 1Developmental disorder
- 1Disorder of skeletal muscle
- 1Genetic disease
- 2Chronic disease
- 2Degenerative disorder
- 2Disease
- 2Disorder of muscle
- 2Disorder of musculoskeletal system
- 2Disorder of soft tissue
- 3Clinical finding
- 3Disorder of body system
- 3General finding of soft tissue
- 3Muscle finding
- 3Musculoskeletal finding
Narrower concepts
(126)Included automatically when you query with descendants.
- 1Emery-Dreifuss muscular dystrophy
- 1Hereditary progressive muscular dystrophy
- 1Muscular dystrophy not predominantly limb girdle in distribution
- 1Scapuloperoneal muscular dystrophy
- 2Autosomal dominant Emery-Dreifuss muscular dystrophy
- 2Autosomal dominant muscular dystrophy not predominantly limb girdle
- 2Autosomal recessive Emery-Dreifuss muscular dystrophy
- 2Autosomal recessive muscular dystrophy not predominantly limb girdle
- 2Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome
- 2Congenital hereditary muscular dystrophy
- 2Distal muscular dystrophy
- 2Muscular dystrophy with predominantly proximal limb girdle distribution
- 2Myotonic dystrophy
- 2Severe childhood autosomal recessive muscular dystrophy
- 2Severe scapuloperoneal muscular dystrophy with cardiomyopathy
- 2X-linked Emery-Dreifuss muscular dystrophy
- 2X-linked muscular dystrophy not predominantly limb girdle
- 2X-linked myopathy with postural muscle atrophy
- 2X-linked scapuloperoneal muscular dystrophy
- 3Adenylosuccinate synthetase-like 1-related distal myopathy
- 3Adult-onset distal myopathy due to valosin containing protein mutation
- 3Autosomal dominant muscular dystrophy with limb girdle distribution
- 3Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein
- 3Autosomal recessive muscular dystrophy with limb girdle distribution
- 3Autosomal recessive myogenic arthrogryposis multiplex congenita
Showing 25 of 126. Retrieve the full set via the API.
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