OMOP Concept 36714550
X-linked distal arthrogryposis multiplex congenita
StandardConditionSNOMED719836007Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to X-linked distal arthrogryposis multiplex congenita via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535380 | Arthrogryposis multiplex congenita, distal, X-linked | Non-standard |
| Nebraska Lexicon | 719836007 | Spinal muscular atrophy with arthrogryposis | Non-standard |
Synonyms
Alternative names recorded for X-linked distal arthrogryposis multiplex congenita across source vocabularies.
- artrogriposis múltiple distal congénita ligada al cromosoma X
- artrogriposis múltiple distal congénita ligada al cromosoma X (trastorno)
- atrofia muscular espinal ligada al cromosoma X tipo 2
- Infantile-onset X-linked spinal muscular atrophy
- Spinal muscular atrophy with arthrogryposis
- X-linked distal arthrogryposis multiplex congenita (disorder)
- X-linked spinal muscular atrophy type 2
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
- 1Inherited arthrogryposis
- 1Spinal muscular atrophy
- 1X-linked distal hereditary motor neuropathy
- 1X-linked recessive hereditary disease
- 2Arthrogryposis
- 2Arthropathy
- 2Chronic disease of musculoskeletal system
- 2Chronic nervous system disorder
- 2Developmental hereditary disorder
- 2Hereditary disorder of musculoskeletal system
- 2Hereditary disorder of nervous system
- 2Hereditary motor neuron disease
- 2Lower motor neuron disease
- 2Peripheral motor neuropathy
- 2X-linked hereditary disease
- 3Chronic disease
- 3Congenital deformity
- 3Contracture of multiple joints
- 3Developmental disorder
- 3Disorder of joint region
- 3Disorder of musculoskeletal system
- 3Disorder of nervous system
- 3Disorder of skeletal system
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