OMOP Concept 37395762
Ehlers-Danlos syndrome classic type
StandardConditionSNOMED715318006Disorder
Maps from
3
Descendants
1
Valid from
31 Jul 2016
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
3 source codes normalize to Ehlers-Danlos syndrome classic type via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 141426 | Ehlers-Danlos syndrome, type 2 | Non-standard |
| CIEL | 141427 | Ehlers-Danlos syndrome, type 1 | Non-standard |
| ICD10CM | Q79.61 | Classical Ehlers-Danlos syndrome | Non-standard |
Synonyms
Alternative names recorded for Ehlers-Danlos syndrome classic type across source vocabularies.
- Classical Ehlers-Danlos syndrome
- Ehlers-Danlos syndrome classical type
- Ehlers-Danlos syndrome classic type (disorder)
- síndrome de Ehlers-Danlos, tipo clásico
- síndrome de Ehlers-Danlos, tipo clásico (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(49)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Ehlers-Danlos syndrome
- 2Autosomal hereditary disorder
- 2Congenital anomaly of skeletal bone
- 2Congenital anomaly of skin
- 2Congenital connective tissue disorder
- 2Connective tissue hereditary disorder
- 2Developmental hereditary disorder
- 2Hereditary disorder of musculoskeletal system
- 2Hereditary disorder of the integument
- 2Lesion of bone
- 2Metabolic bone disease
- 2Metabolic disease of collagen
- 2Musculoskeletal and connective tissue disorder
- 2Skeletal dysplasia
- 2Skin lesion
- 3Congenital anomaly of integument
- 3Congenital anomaly of musculoskeletal system
- 3Congenital disease
- 3Developmental disorder
- 3Disorder of bone
- 3Disorder of bone development
- 3Disorder of connective tissue
- 3Disorder of integument
- 3Disorder of musculoskeletal system
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Narrower concepts
(1)Included automatically when you query with descendants.
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