Ehlers-Danlos syndrome, classical type (Q46616): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Síndrome de Ehlers-Danlos, tipo clássico é um tipo de síndrome de Ehlers-Danlos (SED), um grupo heterogêneo de doenças hereditárias do tecido conjuntivo caracterizadas por hiperfrouxidão articular, hiperelasticidade cutânea e fragilidade tecidual, e é caracterizada pelos seguintes critérios diagnósticos clínicos principais: pele hiperextensível, cicatrizes cutâneas atróficas devidas à fragilidade cutânea e hiperfrouxidão articular.
@@ description / en / description / en @@
+Ehlers-Danlos syndrome, classic type 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 the following major clinical diagnostic criteria: hyperextensible skin, atrophic cutaneous scars due to tissue fragility and joint hyperlaxity.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1724920772
@@ Property / Canonical URI: https://id.who.int/icd/entity/1724920772 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:LD28.10
@@ Property / CURIE: CID11:LD28.10 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-LD28.10
@@ Property / Canary Token: dki-india-LD28.10 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank
@@ Property / Linked ICD 10 @@
+ICD Q223
@@ Property / Linked ICD 10: ICD Q223 / rank @@
+Normal rank

Latest revision as of 15:19, 13 August 2026

Ehlers-Danlos syndrome, classic type 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 the following major clinical diagnostic criteria: hyperextensible skin, atrophic cutaneous scars due to tissue fragility and joint hyperlaxity.

Language	Label	Description	Also known as
default for all languages	LD28.10
English	Ehlers-Danlos syndrome, classical type	Ehlers-Danlos syndrome, classic type 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 the following major clinical diagnostic criteria: hyperextensible skin, atrophic cutaneous scars due to tissue fragility and joint hyperlaxity.