OMOP Concept 37163194
Distal arthrogryposis type 10
StandardConditionSNOMED1208482007Disorder
Maps from
1
Descendants
0
Valid from
31 Mar 2022
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Distal arthrogryposis type 10 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C566069 | Arthrogryposis, Distal, Type 10 | Non-standard |
Synonyms
Alternative names recorded for Distal arthrogryposis type 10 across source vocabularies.
- artrogriposis distal tipo 10
- artrogriposis distal tipo 10 (trastorno)
- Congenital plantar flexion contracture
- contractura en flexión plantar congénita
- DA10 - distal arthrogryposis type 10
- Distal arthrogryposis type 10 (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(60)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital flexion contracture of foot joint
- 1Distal arthrogryposis syndrome
- 1Inherited arthrogryposis
- 2Arthrogryposis
- 2Autosomal hereditary disorder
- 2Congenital deformity of foot
- 2Contracture of joint of foot
- 2Developmental hereditary disorder
- 2Flexion contracture
- 2Genetic disease
- 2Hereditary disorder of musculoskeletal system
- 2Longitudinal deficiency of part of limb
- 3Congenital anomaly of foot
- 3Congenital anomaly of limb
- 3Congenital deformity
- 3Congenital deformity of lower limb
- 3Contracture of joint
- 3Contracture of multiple joints
- 3Decreased range of foot movement
- 3Deformity of foot
- 3Deformity of limb
- 3Developmental disorder
- 3Disease
- 3Disorder of foot
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