OMOP Concept 4284819
X-linked Ehlers-Danlos syndrome
StandardConditionSNOMED67202007Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
3 source codes normalize to X-linked Ehlers-Danlos syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 141423 | Ehlers-Danlos syndrome, type 5 | Non-standard |
| MeSH | C536197 | Ehlers-Danlos syndrome type 5 | Non-standard |
| Read | PGy2400 | Ehlers-Danlos syndrome type V | Non-standard |
Synonyms
Alternative names recorded for X-linked Ehlers-Danlos syndrome across source vocabularies.
- Ehlers-Danlos syndrome, type 5
- Ehlers-Danlos syndrome type V
- síndrome de Ehlers-Danlos ligado a X
- síndrome de Ehlers-Danlos ligado a X (trastorno)
- síndrome de Ehlers Danlos, tipo 5
- síndrome de Ehlers - Danlos, tipo leve ligado al cromosoma X
- X-linked Ehlers-Danlos syndrome (disorder)
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
- 1X-linked recessive hereditary disease
- 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
- 2X-linked hereditary disease
- 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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