Compound heterozygous sickling disorders without crisis (Q39532): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Doença causada por herança genética de dois alelos recessivos heterozigotos do gene da hemoglobina levando à formação anormal da molécula de hemoglobina. Esta doença é caracterizada por glóbulos vermelhos rígidos no formato de foice. A confirmação é feita pela identificação de mutações através de testes genéticos.
@@ description / en / description / en @@
+A disease caused by genetic inheritance of two heterozygous recessive alleles of the haemoglobin gene leading to abnormal formation of haemoglobin molecule. This disease is characterised by rigid, sickle shaped red blood cells. Confirmation is by identification of mutations through genetic testing.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/313446364
@@ Property / Canonical URI: https://id.who.int/icd/entity/313446364 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:3A51.3
@@ Property / CURIE: CID11:3A51.3 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-3A51.3
@@ Property / Canary Token: dki-india-3A51.3 / 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 @@
+D57.2
@@ Property / Linked ICD 10: D57.2 / rank @@
+Normal rank

Latest revision as of 04:59, 13 August 2026

A disease caused by genetic inheritance of two heterozygous recessive alleles of the haemoglobin gene leading to abnormal formation of haemoglobin molecule. This disease is characterised by rigid, sickle shaped red blood cells. Confirmation is by identification of mutations through genetic testing.

Language	Label	Description	Also known as
default for all languages	3A51.3
English	Compound heterozygous sickling disorders without crisis	A disease caused by genetic inheritance of two heterozygous recessive alleles of the haemoglobin gene leading to abnormal formation of haemoglobin molecule. This disease is characterised by rigid, sickle shaped red blood cells. Confirmation is by identification of mutations through genetic testing.