Ehlers-Danlos syndrome, X-linked (Q101840): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed label, description and/or aliases in pt-br, en
‎Changed an Item
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/811572965 / rank
 
Normal rank

Revision as of 18:41, 16 August 2026

Ehlers-Danlos syndrome type 5 is a type of Ehlers-Danlos syndromes (EDS), a heterogeneous group of hereditary connective tissue diseases characterised by joint hyperlaxity, cutaneous hyperelasticity and tissue fragility, and is characterised by hyperextensible skin but tissue fragility and joint hyperlaxity are mild.
Language Label Description Also known as
default for all languages
ID_811572965
    English
    Ehlers-Danlos syndrome, X-linked
    Ehlers-Danlos syndrome type 5 is a type of Ehlers-Danlos syndromes (EDS), a heterogeneous group of hereditary connective tissue diseases characterised by joint hyperlaxity, cutaneous hyperelasticity and tissue fragility, and is characterised by hyperextensible skin but tissue fragility and joint hyperlaxity are mild.

      Statements