OMOP Concept 4009040
Arthrogryposis
StandardConditionSNOMED111246005Disorder
Maps from
11
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
11 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 |
| Nebraska Lexicon | 111246005 | Arthrogryposis | Non-standard |
| Nebraska Lexicon | 253911002 | Multiple congenital articular rigidities | 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
(26)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
- 4Disease
- 4Disorder of fetus and/or newborn
- 4Disorder of skeletal system
- 4Finding of movement
- 4Finding of range of joint movement
- 4Joint finding
- 5Disorder of musculoskeletal system
- 5Finding of joint movement
- 5Musculoskeletal finding
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
- 2Distal arthrogryposis type 3
- 2Distal arthrogryposis type 4
- 2Distal arthrogryposis type 5D
- 2Distal arthrogryposis type 6
- 2Ehlers-Danlos syndrome musculocontractural type
- 2Familial arthrogryposis-cholestatic hepatorenal syndrome
- 2Freeman-Sheldon syndrome
- 2German syndrome
- 2Hecht syndrome
- 2Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome
- 2Hypomyelination neuropathy arthrogryposis syndrome
- 2Illum syndrome
- 2Intellectual disability, developmental delay, contracture syndrome
- 2Kuskokwim syndrome
- 2Larsen-like syndrome B3GAT3 type
- 2Lethal arthrogryposis with anterior horn cell disease
- 2Lethal congenital contracture syndrome type 1
- 2Lethal congenital contracture syndrome type 2
- 2Lethal congenital contracture syndrome type 3
- 2Lethal congenital contracture syndrome type 5
- 2Malignant hyperthermia with arthrogryposis and torticollis syndrome
- 2Marden Walker syndrome
- 2Microphthalmia, microtia, fetal akinesia syndrome
- 2Morse Rawnsley Sargent syndrome
- 2MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome
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