Hereditary persistence of fetal haemoglobin (Q39520): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A persistência hereditária da hemoglobina fetal (HPFH) associada com a beta talassemia é uma hemoglobinopatia caracterizada pelos níveis elevados de hemoglobina (Hb) F e um número aumentado de células contendo Hb fetal. A associação da HPFH com beta talassemia atenua as manifestações clínicas as quais variam de um estado normal a beta talassemia intermédia.
@@ description / en / description / en @@
+Hereditary persistence of fetal haemoglobin (HPFH) associated with beta-thalassaemia is a haemoglobinopathy characterised by high haemoglobin (Hb)F levels and an increased number of fetal-Hb-containing cells. The association of HPFH with beta-thalassaemia mitigates the clinical manifestations which vary from a normal state to beta-thalassaemia intermedia.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/418601307
@@ Property / Canonical URI: https://id.who.int/icd/entity/418601307 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:3A50.4
@@ Property / CURIE: CID11:3A50.4 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-3A50.4
@@ Property / Canary Token: dki-india-3A50.4 / 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 @@
+D56.4
@@ Property / Linked ICD 10: D56.4 / rank @@
+Normal rank

Latest revision as of 04:58, 13 August 2026

Hereditary persistence of fetal haemoglobin (HPFH) associated with beta-thalassaemia is a haemoglobinopathy characterised by high haemoglobin (Hb)F levels and an increased number of fetal-Hb-containing cells. The association of HPFH with beta-thalassaemia mitigates the clinical manifestations which vary from a normal state to beta-thalassaemia intermedia.

Language	Label	Description	Also known as
default for all languages	3A50.4
English	Hereditary persistence of fetal haemoglobin	Hereditary persistence of fetal haemoglobin (HPFH) associated with beta-thalassaemia is a haemoglobinopathy characterised by high haemoglobin (Hb)F levels and an increased number of fetal-Hb-containing cells. The association of HPFH with beta-thalassaemia mitigates the clinical manifestations which vary from a normal state to beta-thalassaemia intermedia.