Sickle cell trait (Q39533): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Doença causada pela herança genética de um alelo anormal do gene da hemoglobina. Esta doença não manifesta os sintomas graves da doença falciforme que ocorre nos indivíduos homozigotos. A confirmação é pela identificação da mutação através do teste genético.
@@ description / en / description / en @@
+A disease caused by genetic inheritance of one abnormal allele of the haemoglobin gene. This disease does not display the severe symptoms of sickle cell disease that occurs in homozygous individuals. Confirmation is by identification of mutation through genetic testing.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/2011497038
@@ Property / Canonical URI: https://id.who.int/icd/entity/2011497038 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:3A51.0
@@ Property / CURIE: CID11:3A51.0 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-3A51.0
@@ Property / Canary Token: dki-india-3A51.0 / 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 @@
+D57.3
@@ Property / Linked ICD 10: D57.3 / rank @@
+Normal rank

Latest revision as of 04:59, 13 August 2026

A disease caused by genetic inheritance of one abnormal allele of the haemoglobin gene. This disease does not display the severe symptoms of sickle cell disease that occurs in homozygous individuals. Confirmation is by identification of mutation through genetic testing.

Language	Label	Description	Also known as
default for all languages	3A51.0
English	Sickle cell trait	A disease caused by genetic inheritance of one abnormal allele of the haemoglobin gene. This disease does not display the severe symptoms of sickle cell disease that occurs in homozygous individuals. Confirmation is by identification of mutation through genetic testing.