OMOP Concept 4344046
Autosomal dominant muscular dystrophy not predominantly limb girdle
StandardConditionSNOMED240075007Disorder
Maps from
1
Descendants
4
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Autosomal dominant muscular dystrophy not predominantly limb girdle via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 240075007 | Autosomal dominant muscular dystrophy not predominantly limb girdle | Non-standard |
Synonyms
Alternative names recorded for Autosomal dominant muscular dystrophy not predominantly limb girdle across source vocabularies.
- Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder)
- distrofia muscular autosómica dominante sin predominio en la cintura de extremidad
- distrofia muscular autosómica dominante sin predominio en la cintura de extremidad (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(33)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital hereditary muscular dystrophy
- 1Muscular dystrophy not predominantly limb girdle in distribution
- 2Autosomal hereditary disorder
- 2Congenital anomaly of skeletal muscle
- 2Hereditary progressive muscular dystrophy
- 2Muscular dystrophy
- 3Chronic disease of musculoskeletal system
- 3Congenital anomaly of muscle AND/OR tendon
- 3Degenerative disorder of muscle
- 3Degenerative disorder of musculoskeletal system
- 3Developmental disorder
- 3Developmental hereditary disorder
- 3Disorder of skeletal muscle
- 3Genetic disease
- 3Hereditary disease
- 3Hereditary disorder of musculoskeletal system
- 4Chronic disease
- 4Congenital anomaly of musculoskeletal system
- 4Degenerative disorder
- 4Disease
- 4Disorder of muscle
- 4Disorder of musculoskeletal system
- 4Disorder of soft tissue
- 4Hereditary disorder by system
Narrower concepts
(4)Included automatically when you query with descendants.
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