MODY 1 syndrome (Q102303): Difference between revisions

← Older edit

@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/289825291
@@ Property / Canonical URI: https://id.who.int/icd/entity/289825291 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_289825291
@@ Property / CURIE: CID11:ID_289825291 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_289825291
@@ Property / Canary Token: dki-india-ID_289825291 / 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 +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-15T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 15 August 2026 / rank @@
+Normal rank

Latest revision as of 19:14, 16 August 2026

This refers to the hereditary form of diabetes caused by mutations in an autosomal dominant gene (sex independent, i.e. inherited from any of the parents) disrupting insulin production. This form is due to a loss-of-function mutation in the HNF4? gene. 5%–10% cases.

Language	Label	Description	Also known as
default for all languages	ID_289825291
English	MODY 1 syndrome	This refers to the hereditary form of diabetes caused by mutations in an autosomal dominant gene (sex independent, i.e. inherited from any of the parents) disrupting insulin production. This form is due to a loss-of-function mutation in the HNF4? gene. 5%–10% cases.