OMOP Concept 37168898
Ehlers-Danlos syndrome classic type 2
StandardConditionSNOMED1287094005Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2023
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Ehlers-Danlos syndrome classic type 2 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536195 | Ehlers-Danlos syndrome type 2 | Non-standard |
| Read | PGy2100 | Ehlers-Danlos syndrome type II | Non-standard |
Synonyms
Alternative names recorded for Ehlers-Danlos syndrome classic type 2 across source vocabularies.
- Ehlers-Danlos syndrome classic type 2 (disorder)
- síndrome de Ehlers Danlos tipo clásico 2
- síndrome de Ehlers Danlos tipo clásico 2 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(50)Roll up to these when you need a wider cohort.
- 1Ehlers-Danlos syndrome classic type
- 2Autosomal dominant hereditary disorder
- 2Ehlers-Danlos syndrome
- 3Autosomal hereditary disorder
- 3Congenital anomaly of skeletal bone
- 3Congenital anomaly of skin
- 3Congenital connective tissue disorder
- 3Connective tissue hereditary disorder
- 3Developmental hereditary disorder
- 3Hereditary disorder of musculoskeletal system
- 3Hereditary disorder of the integument
- 3Lesion of bone
- 3Metabolic bone disease
- 3Metabolic disease of collagen
- 3Musculoskeletal and connective tissue disorder
- 3Skeletal dysplasia
- 3Skin lesion
- 4Congenital anomaly of integument
- 4Congenital anomaly of musculoskeletal system
- 4Congenital disease
- 4Developmental disorder
- 4Disorder of bone
- 4Disorder of bone development
- 4Disorder of connective tissue
- 4Disorder of integument
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