Combined immunodeficiency due to CRAC channel dysfunction (Q88882): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Imunodeficiência combinada (CID) devida a disfunção do canal de Ca2+ ativado por liberação de Ca2+ (CRAC) é uma forma de CID caracterizada por infecções recorrentes, autoimunidade, miopatia congênita e displasia ectodérmica. Compreende dois subtipos que são devidos a mutações nos genes ORAI1 e STIM1: CID devida à deficiência de ORAI1 e CID devida à deficiência de STIM1 (ver estes termos).
@@ description / en / description / en @@
+Combined immunodeficiency (CID) due to Ca2+ release activated Ca2+(CRAC) channel dysfunction is a form of CID characterised by recurrent infections, autoimmunity, congenital myopathy and ectodermal dysplasia. It comprises two sub-types that are due to mutations in the ORAI1 and STIM1 genes: CID due to ORAI1 deficiency and CID due to STIM1 deficiency (see these terms).
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1641826886
@@ Property / Canonical URI: https://id.who.int/icd/entity/1641826886 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_1641826886
@@ Property / CURIE: CID11:ID_1641826886 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_1641826886
@@ Property / Canary Token: dki-india-ID_1641826886 / 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

Latest revision as of 15:16, 15 August 2026

Combined immunodeficiency (CID) due to Ca2+ release activated Ca2+(CRAC) channel dysfunction is a form of CID characterised by recurrent infections, autoimmunity, congenital myopathy and ectodermal dysplasia. It comprises two sub-types that are due to mutations in the ORAI1 and STIM1 genes: CID due to ORAI1 deficiency and CID due to STIM1 deficiency (see these terms).

Language	Label	Description	Also known as
default for all languages	ID_1641826886
English	Combined immunodeficiency due to CRAC channel dysfunction	Combined immunodeficiency (CID) due to Ca2+ release activated Ca2+(CRAC) channel dysfunction is a form of CID characterised by recurrent infections, autoimmunity, congenital myopathy and ectodermal dysplasia. It comprises two sub-types that are due to mutations in the ORAI1 and STIM1 genes: CID due to ORAI1 deficiency and CID due to STIM1 deficiency (see these terms).