Friedreich ataxia (Q41031): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Ataxia de Friedreich é uma ataxia autossômica recessiva caracterizada por dificuldade de coordenação de movimentos associada a sinais neurológicos (disartria, arreflexia, diminuição de sensibilidade profunda, pé cavo e escoliose), cardiomiopatia e as vezes diabetes mellitus. É devido a mutação do gene da frataxina.
@@ description / en / description / en @@
+Friedreich ataxia is an autosomal recessive ataxia characterised by difficulties to coordinate movements, associated with neurological signs (dysarthria, loss of reflexes, decrease of deep sensation, pes cavus and scoliosis), cardiomyopathy and sometimes diabetes mellitus. It is due to a mutation in the frataxin gene.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/980686666
@@ Property / Canonical URI: https://id.who.int/icd/entity/980686666 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:8A03.10
@@ Property / CURIE: CID11:8A03.10 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-8A03.10
@@ Property / Canary Token: dki-india-8A03.10 / 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 @@
+G11
@@ Property / Linked ICD 10: G11 / rank @@
+Normal rank

Latest revision as of 07:04, 13 August 2026

Friedreich ataxia is an autosomal recessive ataxia characterised by difficulties to coordinate movements, associated with neurological signs (dysarthria, loss of reflexes, decrease of deep sensation, pes cavus and scoliosis), cardiomyopathy and sometimes diabetes mellitus. It is due to a mutation in the frataxin gene.

Language	Label	Description	Also known as
default for all languages	8A03.10
English	Friedreich ataxia	Friedreich ataxia is an autosomal recessive ataxia characterised by difficulties to coordinate movements, associated with neurological signs (dysarthria, loss of reflexes, decrease of deep sensation, pes cavus and scoliosis), cardiomyopathy and sometimes diabetes mellitus. It is due to a mutation in the frataxin gene.