Ehlers-Danlos syndrome, classical type

ICD-11 code : LD28.10;

Preferred Label : Ehlers-Danlos syndrome, classical type;

ICD-11 definition : Ehlers-Danlos syndrome, classic type is a type of Ehlers-Danlos syndromes (EDS), a heterogeneous group of hereditary connective tissue diseases characterized by joint hyperlaxity, cutaneous hyperelasticity and tissue fragility, and is characterised by the following major clinical diagnostic criteria: hyperextensible skin, atrophic cutaneous scars due to tissue fragility and joint hyperlaxity.;

Details

Origin ID

1724920772;

UMLS CUI

C4225429;

Currated CISMeF NLP mapping
- Classical Ehlers-Danlos syndrome [ORDO Disease]
- Ehlers-Danlos syndrome classic type (disorder) [SNOMED CT concept]
ICD-10 Mapping
- Ehlers-Danlos syndrome [ICD-10 Sub-category]
See also inter- (CISMeF)
- Ehlers-Danlos syndrome due to tenascin-X deficiency (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ehlers-Danlos syndrome classic type (disorder) [SNOMED CT concept]
Validated automatic mappings to NTBT
- Ehlers-Danlos syndrome [ICD-10 Sub-category]
- Ehlers-Danlos syndrome (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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