Congenital myasthenic syndromes (Q41374): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Síndrome miastênica congênita (SMC) é um grupo heterogêneo de doenças geneticamente determinadas. Existem quatro categorias bem definidas: Síndrome miastênica congênita com defeito pré-sináptico, SMC associada à lâmina basal sináptica, Miastenia congênita com defeito pós-sináptico, SMC com deficiência de glicosilação, e a categoria restante é a de SMC não especificada.
@@ description / en / description / en @@
+Congenital myasthenic syndrome (CMS) is a heterogeneous group of genetically determined diseases. There are four well-defined categories: Congenital myasthenic syndrome with presynaptic defect, Synaptic basal lamina-associated CMS, Congenital myasthenia with postsynaptic defect, CMS with glycosylation deficiency, and the remaining category is that of unidentified CMS.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1515367530
@@ Property / Canonical URI: https://id.who.int/icd/entity/1515367530 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:8C61
@@ Property / CURIE: CID11:8C61 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-8C61
@@ Property / Canary Token: dki-india-8C61 / 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 @@
+G70.2
@@ Property / Linked ICD 10: G70.2 / rank @@
+Normal rank

Latest revision as of 07:31, 13 August 2026

Congenital myasthenic syndrome (CMS) is a heterogeneous group of genetically determined diseases. There are four well-defined categories: Congenital myasthenic syndrome with presynaptic defect, Synaptic basal lamina-associated CMS, Congenital myasthenia with postsynaptic defect, CMS with glycosylation deficiency, and the remaining category is that of unidentified CMS.

Language	Label	Description	Also known as
default for all languages	8C61
English	Congenital myasthenic syndromes	Congenital myasthenic syndrome (CMS) is a heterogeneous group of genetically determined diseases. There are four well-defined categories: Congenital myasthenic syndrome with presynaptic defect, Synaptic basal lamina-associated CMS, Congenital myasthenia with postsynaptic defect, CMS with glycosylation deficiency, and the remaining category is that of unidentified CMS.