OMOP Concept 36674514
Classical-like Ehlers-Danlos syndrome type 1
StandardConditionSNOMED778022009Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2019
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Classical-like Ehlers-Danlos syndrome type 1 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C536193 | Ehlers-Danlos syndrome caused by tenascin-X deficiency | Non-standard |
| MeSH | C536194 | Ehlers-Danlos syndrome type 1 | Non-standard |
| Read | PGy2000 | Ehlers-Danlos syndrome type I | Non-standard |
Synonyms
Alternative names recorded for Classical-like Ehlers-Danlos syndrome type 1 across source vocabularies.
- Classical-like Ehlers-Danlos syndrome type 1 (disorder)
- Ehlers-Danlos syndrome classic-like type
- Ehlers-Danlos syndrome due to tenascin-X deficiency
- síndrome de Ehlers-Danlos por deficiencia de tenascina X
- síndrome Ehlers-Danlos similar a clásico tipo 1
- síndrome Ehlers-Danlos similar a clásico tipo 1 (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 recessive 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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