OMOP Concept 4009040
Arthrogryposis
StandardConditionSNOMED111246005Disorder
Maps from
9
Descendants
60
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
9 source codes normalize to Arthrogryposis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 121461 | Pterygoarthromyodysplasia Syndrome | Non-standard |
| CIEL | 121462 | Guerin-Stern syndrome | Non-standard |
| CIEL | 121463 | Arthrogryposis | Non-standard |
| OXMIS | 729 JG | ARTHROGRYPOSIS | Non-standard |
| Read | N233000 | Arthrogryposis | Non-standard |
| Read | PE8y500 | Guerin - Stern syndrome | Non-standard |
| Read | PE8yz12 | Multiple congenital articular rigidities | Non-standard |
| Read | PFy2.00 | Arthrogryposis, unspecified | Non-standard |
| Read | PFy4.00 | Other arthrogryposis syndromes | Non-standard |
Synonyms
Alternative names recorded for Arthrogryposis across source vocabularies.
- Arthrogryposis (disorder)
- artrogrifosis
- artrogriposis
- artrogriposis (trastorno)
- síndrome de Guerin-Stern
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(27)Roll up to these when you need a wider cohort.
- 1Congenital deformity
- 1Contracture of multiple joints
- 2Congenital malformation
- 2Contracture of joint
- 2Deformity
- 2Lesion of joint
- 2Multiple joint deformity
- 2Polyarthropathy
- 3Arthropathy
- 3Clinical finding
- 3Congenital disease
- 3Developmental disorder
- 3Disorder of joint region
- 3Joint deformity
- 3Limitation of joint movement
- 3Movement disorder
- 3Structural abnormality of skeleton
- 4Disease
- 4Disorder of skeletal system
- 4Fetal and/or neonatal disorder
- 4Finding of movement
- 4Finding of range of joint movement
- 4Joint finding
- 5Disorder of musculoskeletal system
- 5Finding of joint movement
Showing 25 of 27. Retrieve the full set via the API.
Narrower concepts
(60)Included automatically when you query with descendants.
- 1Arthrogryposis multiplex congenita
- 1Congenital amyoplasia
- 1Congenital arthrogryposis caused by teratogen
- 1Congenital arthrogryposis due to Akabane virus
- 1Distal arthrogryposis syndrome
- 1Inherited arthrogryposis
- 2Aase Smith type 1 syndrome
- 2Adducted thumbs and arthrogryposis syndrome Christian type
- 2Alkuraya Kucinskas syndrome
- 2Antenatal multi-minicore disease with arthrogryposis multiplex congenita
- 2Arthrogryposis and ectodermal dysplasia syndrome
- 2Arthrogryposis hyperkeratosis syndrome lethal form
- 2Arthrogryposis with oculomotor limitation and electroretinal anomaly
- 2Autism spectrum disorder, epilepsy, arthrogryposis syndrome
- 2Autosomal dominant multiple pterygium syndrome
- 2Autosomal recessive myogenic arthrogryposis multiplex congenita
- 2Camptobrachydactyly
- 2Congenital contractural arachnodactyly
- 2Congenital contracture of limbs and face, hypotonia, developmental delay syndrome
- 2Congenital lethal myopathy Compton North type
- 2Congenital muscular dystrophy with arthrogryposis multiplex congenita
- 2Congenital pontocerebellar hypoplasia type 12
- 2Contracture with ectodermal dysplasia and orofacial cleft syndrome
- 2Digitotalar dysmorphism
- 2Distal arthrogryposis type 10
Showing 25 of 60. Retrieve the full set via the API.
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