Mitochondrial myopathies (Q41402): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Miopatias mitocondriais são um grupo heterogêneo de transtornos causados por disfunção da fosforilação oxidativa mitocondrial e podem ser classificadas de acordo com os defeitos bioquímicos, genéticos (no DNA mitocondrial ou em proteínas codificadas pelo núcleo) associados ou fenótipo clínico. Exclui: defeitos da cadeia respiratória mitocondrial, síndrome de Kearns-Sayre, epilepsia mioclônica com fibras vermelhas irregulares (MERRF)
@@ description / en / description / en @@
+Mitochondrial myopathies are heterogeneous group of disorders caused by dysfunction of mitochondrial oxidative phosphorylation and can be classified according to the associated biochemical, genetic defects (in the mitochondrial DNA or in nuclear encoded proteins) or clinical phenotype. Exclude: defects of mitochondrial respiratory chain, Kearns-Sayre syndrome, myoclonic epilepsy with ragged red fibres (MERRF)
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/601991549
@@ Property / Canonical URI: https://id.who.int/icd/entity/601991549 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:8C73
@@ Property / CURIE: CID11:8C73 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-8C73
@@ Property / Canary Token: dki-india-8C73 / 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 @@
+G71.3
@@ Property / Linked ICD 10: G71.3 / rank @@
+Normal rank

Latest revision as of 07:33, 13 August 2026

Mitochondrial myopathies are heterogeneous group of disorders caused by dysfunction of mitochondrial oxidative phosphorylation and can be classified according to the associated biochemical, genetic defects (in the mitochondrial DNA or in nuclear encoded proteins) or clinical phenotype. Exclude: defects of mitochondrial respiratory chain, Kearns-Sayre syndrome, myoclonic epilepsy with ragged red fibres (MERRF)

Language	Label	Description	Also known as
default for all languages	8C73
English	Mitochondrial myopathies	Mitochondrial myopathies are heterogeneous group of disorders caused by dysfunction of mitochondrial oxidative phosphorylation and can be classified according to the associated biochemical, genetic defects (in the mitochondrial DNA or in nuclear encoded proteins) or clinical phenotype. Exclude: defects of mitochondrial respiratory chain, Kearns-Sayre syndrome, myoclonic epilepsy with ragged red fibres (MERRF)