OMOP Concept 4183129
Multiple joint deformity
StandardConditionSNOMED298147006Clinical Finding
Maps from
1
Descendants
67
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 Multiple joint deformity via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 298147006 | Multiple joint deformity | Non-standard |
Synonyms
Alternative names recorded for Multiple joint deformity across source vocabularies.
- deformidad articular múltiple
- deformidad articular múltiple (hallazgo)
- Multiple joint deformity (finding)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(5)Roll up to these when you need a wider cohort.
Narrower concepts
(67)Included automatically when you query with descendants.
- 1Contracture of multiple joints
- 2Arthrogryposis
- 2Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome
- 2Diastrophic dysplasia
- 2Flexion contracture of proximal interphalangeal joints of index, middle, ring and little finger
- 2Myopathic Ehlers-Danlos syndrome
- 2Spondyloepiphyseal dysplasia Stanescu type
- 3Arthrogryposis multiplex congenita
- 3Congenital amyoplasia
- 3Congenital arthrogryposis caused by teratogen
- 3Congenital arthrogryposis due to Akabane virus
- 3Distal arthrogryposis syndrome
- 3Inherited arthrogryposis
- 4Aase Smith type 1 syndrome
- 4Adducted thumbs and arthrogryposis syndrome Christian type
- 4Alkuraya Kucinskas syndrome
- 4Antenatal multi-minicore disease with arthrogryposis multiplex congenita
- 4Arthrogryposis and ectodermal dysplasia syndrome
- 4Arthrogryposis hyperkeratosis syndrome lethal form
- 4Arthrogryposis with oculomotor limitation and electroretinal anomaly
- 4Autism spectrum disorder, epilepsy, arthrogryposis syndrome
- 4Autosomal dominant multiple pterygium syndrome
- 4Autosomal recessive myogenic arthrogryposis multiplex congenita
- 4Camptobrachydactyly
- 4Congenital contractural arachnodactyly
- 4Congenital contracture of limbs and face, hypotonia, developmental delay syndrome
- 4Congenital lethal myopathy Compton North type
- 4Congenital muscular dystrophy with arthrogryposis multiplex congenita
- 4Congenital pontocerebellar hypoplasia type 12
- 4Contracture with ectodermal dysplasia and orofacial cleft syndrome
- 4Digitotalar dysmorphism
- 4Distal arthrogryposis type 10
- 4Distal arthrogryposis type 3
- 4Distal arthrogryposis type 4
- 4Distal arthrogryposis type 5D
- 4Distal arthrogryposis type 6
- 4Ehlers-Danlos syndrome musculocontractural type
- 4Familial arthrogryposis-cholestatic hepatorenal syndrome
- 4Freeman-Sheldon syndrome
- 4German syndrome
- 4Hecht syndrome
- 4Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome
- 4Hypomyelination neuropathy arthrogryposis syndrome
- 4Illum syndrome
- 4Intellectual disability, developmental delay, contracture syndrome
- 4Kuskokwim syndrome
- 4Larsen-like syndrome B3GAT3 type
- 4Lethal arthrogryposis with anterior horn cell disease
- 4Lethal congenital contracture syndrome type 1
- 4Lethal congenital contracture syndrome type 2
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