OMOP Concept 37164984
Dermatosparaxis Ehlers-Danlos syndrome
StandardConditionSNOMED1237225007Disorder
Maps from
1
Descendants
0
Valid from
31 Aug 2022
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Dermatosparaxis Ehlers-Danlos syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C567527 | Ehlers-Danlos Syndrome, Type VII, Autosomal Recessive | Non-standard |
Synonyms
Alternative names recorded for Dermatosparaxis Ehlers-Danlos syndrome across source vocabularies.
- Dermatosparaxis EDS (Ehlers-Danlos syndrome)
- Dermatosparaxis Ehlers-Danlos syndrome (disorder)
- Ehlers-Danlos syndrome type 7C
- Human dermatosparaxis EDS VIIC (Ehlers-Danlos syndrome type 7C)
- SED (síndrome de Ehlers-Danlos) dermatosparaxis
- SED (síndrome de Ehlers-Danlos) VIIC dermatosparaxis humana
- síndrome de Ehlers-Danlos dermatosparaxis
- síndrome de Ehlers-Danlos dermatosparaxis (trastorno)
- síndrome de Ehlers-Danlos tipo 7C
- síndrome de Ehlers Danlos tipo dermatosparaxis
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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