OMOP Concept 37396015
Multiple epiphyseal dysplasia type 5
StandardConditionSNOMED715674008Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Multiple epiphyseal dysplasia type 5 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535505 | Epiphyseal dysplasia, multiple, 5 | Non-standard |
| Nebraska Lexicon | 715674008 | Multiple epiphyseal dysplasia type 5 | Non-standard |
Synonyms
Alternative names recorded for Multiple epiphyseal dysplasia type 5 across source vocabularies.
- displasia epifisaria múltiple tipo 5
- displasia epifisaria múltiple tipo 5 (trastorno)
- Multiple epiphyseal dysplasia type 5 (disorder)
- Polyepiphyseal dysplasia type 5
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(41)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Multiple epiphyseal dysplasia
- 2Autosomal hereditary disorder
- 2Epiphyseal dysplasia
- 2Spondyloepiphyseal dysplasia tarda
- 3Chronic disease of musculoskeletal system
- 3Congenital anomaly of skeletal bone
- 3Developmental hereditary disorder
- 3Disorder of epiphysis
- 3Hereditary disease
- 3Hereditary disorder of musculoskeletal system
- 3Osteochondrodysplasia syndrome
- 3Skeletal dysplasia
- 3Spondyloepimetaphyseal disorder
- 4Chronic disease
- 4Congenital anomaly of musculoskeletal system
- 4Developmental disorder
- 4Disorder of bone
- 4Disorder of bone development
- 4Disorder of musculoskeletal system
- 4Disorder of skeletal system
- 4Genetic disease
- 4Hereditary disorder by system
- 4Metaphyseal chondrodysplasia
- 4Multiple system malformation syndrome
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