OMOP Concept 4344281
Congenital muscular dystrophy with arthrogryposis multiplex congenita
StandardConditionSNOMED240061000Disorder
Maps from
1
Descendants
0
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 Congenital muscular dystrophy with arthrogryposis multiplex congenita via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 240061000 | Congenital muscular dystrophy with arthrogryposis multiplex congenita | Non-standard |
Synonyms
Alternative names recorded for Congenital muscular dystrophy with arthrogryposis multiplex congenita across source vocabularies.
- Congenital muscular dystrophy with arthrogryposis multiplex congenita (disorder)
- distrofia muscular congénita con artrogriposis múltiple congénita
- distrofia muscular congénita con artrogriposis múltiple congénita (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(51)Roll up to these when you need a wider cohort.
- 1Arthrogryposis multiplex congenita
- 1Chronic arthropathy
- 1Congenital hereditary muscular dystrophy
- 1Inherited arthrogryposis
- 2Arthrogryposis
- 2Arthropathy
- 2Chronic disease of musculoskeletal system
- 2Congenital anomaly of skeletal muscle
- 2Developmental hereditary disorder
- 2Hereditary disorder of musculoskeletal system
- 2Hereditary progressive muscular dystrophy
- 3Chronic disease
- 3Congenital anomaly of muscle AND/OR tendon
- 3Congenital deformity
- 3Contracture of multiple joints
- 3Developmental disorder
- 3Disorder of joint region
- 3Disorder of musculoskeletal system
- 3Disorder of skeletal muscle
- 3Disorder of skeletal system
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Joint finding
- 3Muscular dystrophy
- 4Congenital anomaly of musculoskeletal system
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