Ehlers-Danlos syndrome, arthrochalasic type

Preferred Label : Ehlers-Danlos syndrome, arthrochalasic type;

ICD-11 definition : Ehlers-Danlos syndrome, arthrochalasic 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 marked by bilateral congenital hip dislocation, hyperlaxity of the joints, and recurrent partial dislocations. Other signs include hyperextensible skin, fragile tissues with atrophic scars, and muscular hypotonia.;

ICD-11 synonym : Ehlers-Danlos syndrome type 7;

Details

Origin ID

96808187;

Automatic exact mappings (from CISMeF team)
- Arthrochalasia Ehlers-Danlos syndrome [ORDO Disease]
- Ehlers-Danlos syndrome, procollagen proteinase deficient (disorder) [SNOMED CT concept]
- Ehlers-Danlos syndrome, type VII, autosomal dominant [MeSH concept]
- Ehlers-Danlos syndrome, type VII, autosomal dominant [MeSH Supplementary Concept]
- Ehlers-danlos syndrome, arthrochalasia type, 1 [OMIM Phenotype]

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