OMOP Concept 80399
Hereditary progressive muscular dystrophy
StandardConditionSNOMED193225000Disorder
Maps from
4
Descendants
118
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
4 source codes normalize to Hereditary progressive muscular dystrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138743 | Hereditary progressive muscular dystrophy | Non-standard |
| ICD9CM | 359.1 | Hereditary progressive muscular dystrophy | Non-standard |
| Nebraska Lexicon | 193225000 | Hereditary progressive muscular dystrophy | Non-standard |
| Read | F391.00 | Hereditary progressive muscular dystrophy | Non-standard |
Synonyms
Alternative names recorded for Hereditary progressive muscular dystrophy across source vocabularies.
- Hereditary progressive muscular dystrophy (disorder)
- miodistrofia progresiva hereditaria
- miodistrofia progresiva hereditaria (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(22)Roll up to these when you need a wider cohort.
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Muscular dystrophy
- 2Chronic disease of musculoskeletal system
- 2Degenerative disorder of muscle
- 2Degenerative disorder of musculoskeletal system
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Disorder of skeletal muscle
- 2Genetic disease
- 2Hereditary disease
- 2Hereditary disorder by system
- 3Chronic disease
- 3Degenerative disorder
- 3Disease
- 3Disorder of body system
- 3Disorder of muscle
- 3Disorder of soft tissue
- 3Musculoskeletal finding
- 4Clinical finding
- 4General finding of soft tissue
- 4Muscle finding
Narrower concepts
(118)Included automatically when you query with descendants.
- 1Autosomal dominant Emery-Dreifuss muscular dystrophy
- 1Autosomal recessive Emery-Dreifuss muscular dystrophy
- 1Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome
- 1Congenital hereditary muscular dystrophy
- 1Distal muscular dystrophy
- 1Muscular dystrophy with predominantly proximal limb girdle distribution
- 1Myotonic dystrophy
- 1Severe childhood autosomal recessive muscular dystrophy
- 1X-linked Emery-Dreifuss muscular dystrophy
- 1X-linked myopathy with postural muscle atrophy
- 1X-linked scapuloperoneal muscular dystrophy
- 2Adenylosuccinate synthetase-like 1-related distal myopathy
- 2Adult-onset distal myopathy due to valosin containing protein mutation
- 2Autosomal dominant muscular dystrophy not predominantly limb girdle
- 2Autosomal dominant muscular dystrophy with limb girdle distribution
- 2Autosomal recessive muscular dystrophy not predominantly limb girdle
- 2Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein
- 2Autosomal recessive muscular dystrophy with limb girdle distribution
- 2Autosomal recessive myogenic arthrogryposis multiplex congenita
- 2Benign congenital muscular dystrophy with finger flexion contractures
- 2Bethlem myopathy
- 2Congenital muscular dystrophy due to LMNA mutation
- 2Congenital muscular dystrophy Paradas type
- 2Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome
- 2Congenital muscular dystrophy type 1A
- 2Congenital muscular dystrophy type 1B
- 2Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation
- 2Congenital muscular dystrophy type 1D large gene mutation
- 2Congenital muscular dystrophy with arthrogryposis multiplex congenita
- 2Congenital muscular dystrophy with cerebellar involvement
- 2Congenital muscular dystrophy with hyperlaxity
- 2Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
- 2Congenital muscular dystrophy with integrin alpha-7 deficiency
- 2Congenital muscular dystrophy with intellectual disability
- 2Congenital muscular dystrophy with intellectual disability and severe epilepsy
- 2Congenital muscular dystrophy without intellectual disability
- 2Congenital muscular hypertrophy-cerebral syndrome
- 2Congenital myotonic 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
- 2Early onset myopathy with fatal cardiomyopathy
- 2Eichsfeld type congenital muscular dystrophy
- 2Epidermolysis bullosa simplex with muscular dystrophy
- 2Finnish upper limb onset distal myopathy
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