Fragile X chromosome (Q46933): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A síndrome do X frágil é uma doença genética rara associada a déficit intelectual leve a grave que pode estar associada a transtornos comportamentais e características físicas distintas.
@@ description / en / description / en @@
+Fragile X syndrome is a rare genetic disease associated with mild to severe intellectual deficit that may be associated with behavioural disorders and characteristic physical features.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1524287677
@@ Property / Canonical URI: https://id.who.int/icd/entity/1524287677 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:LD55
@@ Property / CURIE: CID11:LD55 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-LD55
@@ Property / Canary Token: dki-india-LD55 / 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 @@
+Q99.2
@@ Property / Linked ICD 10: Q99.2 / rank @@
+Normal rank

Latest revision as of 15:50, 13 August 2026

Fragile X syndrome is a rare genetic disease associated with mild to severe intellectual deficit that may be associated with behavioural disorders and characteristic physical features.

Language	Label	Description	Also known as
default for all languages	LD55
English	Fragile X chromosome	Fragile X syndrome is a rare genetic disease associated with mild to severe intellectual deficit that may be associated with behavioural disorders and characteristic physical features.