OMOP Concept 4205583
Arthrochalasia Ehlers-Danlos syndrome
StandardConditionSNOMED55711009Disorder
Maps from
4
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
4 source codes normalize to Arthrochalasia Ehlers-Danlos syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 141429 | Ehlers-Danlos Syndrome, Procollagen Proteinase Resistant | Non-standard |
| CIEL | 141430 | Ehlers-Danlos Syndrome, Procollagen Proteinase Deficient | Non-standard |
| MeSH | C562625 | Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant | Non-standard |
| Read | PGy2600 | Ehlers-Danlos syndrome type VII | Non-standard |
Synonyms
Alternative names recorded for Arthrochalasia Ehlers-Danlos syndrome across source vocabularies.
- Arthrochalasia Ehlers-Danlos syndrome (disorder)
- Arthrochalasia multiplex congenita
- Arthrochalasis multiplex congenita
- artrocalasis múltiple congénita
- deficiencia de procolágeno aminoproteasa
- deficiencia de procolágeno peptidasa
- deficiencia de procolágeno proteasa
- Ehlers-Danlos syndrome type 7
- síndrome de Ehlers-Danlos artrocalasia
- síndrome de Ehlers-Danlos artrocalasia (trastorno)
- síndrome de Ehlers - Danlos, autosómico recesivo tipo 7
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(52)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Ehlers-Danlos syndrome
- 1Enzymopathy
- 1Inborn error of metabolism
- 2Autosomal hereditary disorder
- 2Congenital anomaly of skeletal bone
- 2Congenital anomaly of skin
- 2Congenital connective tissue disorder
- 2Congenital disease
- 2Connective tissue hereditary disorder
- 2Developmental hereditary disorder
- 2Hereditary disorder of musculoskeletal system
- 2Hereditary disorder of the integument
- 2Hereditary metabolic disease
- 2Lesion of bone
- 2Metabolic bone disease
- 2Metabolic disease
- 2Metabolic disease of collagen
- 2Musculoskeletal and connective tissue disorder
- 2Skeletal dysplasia
- 2Skin lesion
- 3Congenital anomaly of integument
- 3Congenital anomaly of musculoskeletal system
- 3Developmental disorder
- 3Disease
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