Congenital hypothyroidism due to dual oxidase 2 mutation (Q92180): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Hipotiroidismo congênito devido a mutações de mutações bialélicas de DUOX2
@@ description / en / description / en @@
+Congenital hypothyroidism due to mutations of bialleric mutations of DUOX2
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/679428669
@@ Property / Canonical URI: https://id.who.int/icd/entity/679428669 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_679428669
@@ Property / CURIE: CID11:ID_679428669 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_679428669
@@ Property / Canary Token: dki-india-ID_679428669 / 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 07:20, 16 August 2026

Congenital hypothyroidism due to mutations of bialleric mutations of DUOX2

Language	Label	Description	Also known as
default for all languages	ID_679428669
English	Congenital hypothyroidism due to dual oxidase 2 mutation	Congenital hypothyroidism due to mutations of bialleric mutations of DUOX2