OMOP Concept 80399
Hereditary progressive muscular dystrophy
StandardConditionSNOMED193225000Disorder
Maps from
3
Descendants
121
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
3 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 |
| 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
(121)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
Showing 25 of 121. Retrieve the full set via the API.
Get this concept via the API
Resolve Hereditary progressive muscular dystrophy - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/80399?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card