OMOP Concept 4172671
Severe childhood autosomal recessive muscular dystrophy
StandardConditionSNOMED277373000Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Severe childhood autosomal recessive muscular dystrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 277373000 | Severe childhood autosomal recessive muscular dystrophy | Non-standard |
Synonyms
Alternative names recorded for Severe childhood autosomal recessive muscular dystrophy across source vocabularies.
- distrofia muscular grave autosómica recesiva de la infancia
- distrofia muscular grave autosómica recesiva de la infancia (trastorno)
- miodistrofia infantil grave autosómica recesiva
- SCARMD - Severe childhood autosomal recessive muscular dystrophy
- Severe childhood autosomal recessive muscular dystrophy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(25)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Hereditary progressive muscular dystrophy
- 2Autosomal hereditary disorder
- 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
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