OMOP Concept 4307651
Ehlers-Danlos syndrome, dysfibronectinemic
StandardConditionSNOMED83586000Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Ehlers-Danlos syndrome, dysfibronectinemic via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 141433 | Ehlers-Danlos syndrome, dysfibronectinemic | Non-standard |
| Nebraska Lexicon | 83586000 | Ehlers-Danlos syndrome, dysfibronectinaemic | Non-standard |
Synonyms
Alternative names recorded for Ehlers-Danlos syndrome, dysfibronectinemic across source vocabularies.
- Ehlers-Danlos syndrome, dysfibronectinaemic
- Ehlers-Danlos syndrome, dysfibronectinemic (disorder)
- Ehlers-Danlos syndrome, type 10
- Ehlers-Danlos syndrome with platelet dysfunction
- síndrome de Ehlers - Danlos con disfunción plaquetaria
- síndrome de Ehlers - Danlos, tipo 10
- síndrome de Ehlers-Danlos, variante con alteración de la fibronectina
- síndrome de Ehlers-Danlos, variante con alteración de la fibronectina (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(45)Roll up to these when you need a wider cohort.
- 1Ehlers-Danlos syndrome
- 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
- 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
- 3Disorder of skeletal system
- 3Disorder of skin
- 3Hereditary disease
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