Thalassaemias (Q39512): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Doença causada por mutações autossômicas recessivas geneticamente herdadas levando à produção anormal de hemoglobina. Esta doença é caracterizada pela destruição dos glóbulos vermelhos levando a anemia e produção anormal de hemoglobina. Esta doença pode se manifestar com palidez, icterícia, sobrecarga de ferro, fadiga ou falta de ar. A confirmação é feita pela identificação das mutações por testagem genética.
@@ description / en / description / en @@
+A disease caused by genetically inherited autosomal recessive mutations leading to abnormal production of haemoglobin. This disease is characterised by destruction of red blood cells leading to anaemia and abnormal production of haemoglobin. This disease may present with pallor, jaundice, iron overload, fatigue, or shortness of breath. Confirmation is by identification of mutations through genetic testing.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/330259189
@@ Property / Canonical URI: https://id.who.int/icd/entity/330259189 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:3A50
@@ Property / CURIE: CID11:3A50 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-3A50
@@ Property / Canary Token: dki-india-3A50 / 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 @@
+D56
@@ Property / Linked ICD 10: D56 / rank @@
+Normal rank

Latest revision as of 04:57, 13 August 2026

A disease caused by genetically inherited autosomal recessive mutations leading to abnormal production of haemoglobin. This disease is characterised by destruction of red blood cells leading to anaemia and abnormal production of haemoglobin. This disease may present with pallor, jaundice, iron overload, fatigue, or shortness of breath. Confirmation is by identification of mutations through genetic testing.

Language	Label	Description	Also known as
default for all languages	3A50
English	Thalassaemias	A disease caused by genetically inherited autosomal recessive mutations leading to abnormal production of haemoglobin. This disease is characterised by destruction of red blood cells leading to anaemia and abnormal production of haemoglobin. This disease may present with pallor, jaundice, iron overload, fatigue, or shortness of breath. Confirmation is by identification of mutations through genetic testing.