OMOP Concept 4247802
Muscular dystrophy
StandardConditionSNOMED73297009Disorder
Maps from
35
Descendants
123
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
35 source codes normalize to Muscular dystrophy via the OMOP "Maps to" relationship.
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
(123)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
- 3Benign congenital muscular dystrophy with finger flexion contractures
- 3Benign scapuloperoneal muscular dystrophy
- 3Bethlem myopathy
- 3Congenital muscular dystrophy due to LMNA mutation
- 3Congenital muscular dystrophy Paradas type
- 3Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome
- 3Congenital muscular dystrophy type 1A
- 3Congenital muscular dystrophy type 1B
- 3Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation
- 3Congenital muscular dystrophy type 1D large gene mutation
- 3Congenital muscular dystrophy with arthrogryposis multiplex congenita
- 3Congenital muscular dystrophy with cerebellar involvement
- 3Congenital muscular dystrophy with hyperlaxity
- 3Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
- 3Congenital muscular dystrophy with integrin alpha-7 deficiency
- 3Congenital muscular dystrophy with intellectual disability
- 3Congenital muscular dystrophy with intellectual disability and severe epilepsy
- 3Congenital muscular dystrophy without intellectual disability
- 3Congenital muscular hypertrophy-cerebral syndrome
- 3Congenital myotonic dystrophy
- 3Distal anoctaminopathy
- 3Distal muscular dystrophy, Miyoshi type
- 3Distal muscular dystrophy with juvenile onset
- 3Distal myopathy 2
- 3Distal myopathy Welander type
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