OMOP Concept 36713987
Upington disease
StandardConditionSNOMED719041000Disorder
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 Upington disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536472 | Upington disease | Non-standard |
| Nebraska Lexicon | 719041000 | Hip dysplasia with enchondromata and ecchondroma syndrome | Non-standard |
Synonyms
Alternative names recorded for Upington disease across source vocabularies.
- Hip dysplasia with enchondromata and ecchondroma syndrome
- Hip dysplasia with enchondromata and ecchondroma syndrome (disorder)
- síndrome de displasia de cadera con encondromas u osteocondromas
- síndrome de displasia de cadera con encondromas u osteocondromas (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(70)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital hip dysplasia
- 1Connective tissue hereditary disorder
- 1Developmental hereditary disorder
- 1Disorganized development of cartilaginous and fibrous components of the skeleton
- 1Hereditary disorder of musculoskeletal system
- 1Osteochondropathy
- 2Autosomal hereditary disorder
- 2Cartilage disorder
- 2Congenital anomaly of bone and joint
- 2Congenital anomaly of cartilage
- 2Congenital anomaly of pelvic bones
- 2Congenital dysplasia of lower limb
- 2Developmental disorder
- 2Disorder of bone
- 2Disorder of connective tissue
- 2Disorder of hip joint
- 2Disorder of musculoskeletal system
- 2Disorder of pelvic girdle
- 2Finding of bone of lower limb
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Lesion of joint
- 2Skeletal dysplasia
- 3Arthropathy
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