Mevalonate kinase deficiency with recurrent fever (Q88717): Difference between revisions

← Older edit

@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/910632716
@@ Property / Canonical URI: https://id.who.int/icd/entity/910632716 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_910632716
@@ Property / CURIE: CID11:ID_910632716 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_910632716
@@ Property / Canary Token: dki-india-ID_910632716 / 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 15:06, 15 August 2026

Mevalonate kinase [MVK] deficiency with recurrent fever, with or without hyperIgD, is an autoinflammatory disease associated with mutations in the mevalonate kinase gene. This results in clinical attacks of inflammation in the form of fever, lymphadenopathy, enlarged spleen and serositis along with increased acute phase reactants.

Language	Label	Description	Also known as
default for all languages	ID_910632716
English	Mevalonate kinase deficiency with recurrent fever	Mevalonate kinase [MVK] deficiency with recurrent fever, with or without hyperIgD, is an autoinflammatory disease associated with mutations in the mevalonate kinase gene. This results in clinical attacks of inflammation in the form of fever, lymphadenopathy, enlarged spleen and serositis along with increased acute phase reactants.