Familial-genetic dilated cardiomyopathy (Q42357): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Cardiomiopatia dilatada genética familiar é a presença de cardiomiopatia dilatada que está presente em vários membros de uma linhagem, ou na presença de uma mutação genética conhecida por estar significativamente associada a cardiomiopatia dilatada. _x000D_ _x000D_ Informações adicionais: Genes candidatos do citoesqueleto e codificadores do disco Z, a maioria dos quais são aventados como responsáveis por anormalidades na transmissão de força, incluem δ-sarcoglicano, β-sarcoglicano, desmina, lamina A / C, metavinculina, proteína LIM muscular, titina, α -actinina-2, nebuleta, miopaladina e ZASP (proteína de domínio PDZ com “splicing” alternativo de banda Z)
@@ description / en / description / en @@
+Familial-genetic dilated cardiomyopathy is the presence of dilated cardiomyopathy that is present in multiple members of a pedigree, or in the presence of a genetic mutation known to be significantly associated with dilated cardiomyopathy. Additional information: Candidate cytoskeletal and Z disk–encoding genes, most of whom are hypothesized to lead to abnormalities in force transmission, include δ-sarcoglycan, β-sarcoglycan, desmin, lamin A/C, metavinculin, muscle LIM protein, titin, α-actinin-2, nebulette, myopalladin, and ZASP (Z band alternatively spliced PDZ domain protein)
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/423719003
@@ Property / Canonical URI: https://id.who.int/icd/entity/423719003 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:BC43.00
@@ Property / CURIE: CID11:BC43.00 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-BC43.00
@@ Property / Canary Token: dki-india-BC43.00 / 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 @@
+I42.0
@@ Property / Linked ICD 10: I42.0 / rank @@
+Normal rank

Latest revision as of 08:50, 13 August 2026

Familial-genetic dilated cardiomyopathy is the presence of dilated cardiomyopathy that is present in multiple members of a pedigree, or in the presence of a genetic mutation known to be significantly associated with dilated cardiomyopathy. Additional information: Candidate cytoskeletal and Z disk–encoding genes, most of whom are hypothesized to lead to abnormalities in force transmission, include δ-sarcoglycan, β-sarcoglycan, desmin, lamin A/C, metavinculin, muscle LIM protein, titin, α-actinin-2, nebulette, myopalladin, and ZASP (Z band alternatively spliced PDZ domain protein)

Language	Label	Description	Also known as
default for all languages	BC43.00
English	Familial-genetic dilated cardiomyopathy	Familial-genetic dilated cardiomyopathy is the presence of dilated cardiomyopathy that is present in multiple members of a pedigree, or in the presence of a genetic mutation known to be significantly associated with dilated cardiomyopathy. Additional information: Candidate cytoskeletal and Z disk–encoding genes, most of whom are hypothesized to lead to abnormalities in force transmission, include δ-sarcoglycan, β-sarcoglycan, desmin, lamin A/C, metavinculin, muscle LIM protein, titin, α-actinin-2, nebulette, myopalladin, and ZASP (Z band alternatively spliced PDZ domain protein)