Sickle cell disease without crisis (Q39531): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Transtorno causado por uma mutação HbS no gene da hemoglobina. Este transtorno é caracterizado por hemácias anormais rígidas em forma de foice diminuindo sua capacidade de transportar oxigênio. Este transtorno pode se manifestar com fadiga, falta de ar, tonturas, dores de cabeça, palidez de pele ou mucosas, e icterícia. Este transtorno é confirmado pela identificação da mutação HbS por testes genéticos.
@@ description / en / description / en @@
+A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may present with fatigue, shortness of breath, dizziness, headaches, pallor of skin or mucous membranes, and jaundice. This disorder is confirmed by identification of HbS mutation by genetic testing.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1711513381
@@ Property / Canonical URI: https://id.who.int/icd/entity/1711513381 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:3A51.1
@@ Property / CURIE: CID11:3A51.1 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-3A51.1
@@ Property / Canary Token: dki-india-3A51.1 / 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 @@
+D57.1
@@ Property / Linked ICD 10: D57.1 / rank @@
+Normal rank

Latest revision as of 04:59, 13 August 2026

A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may present with fatigue, shortness of breath, dizziness, headaches, pallor of skin or mucous membranes, and jaundice. This disorder is confirmed by identification of HbS mutation by genetic testing.

Language	Label	Description	Also known as
default for all languages	3A51.1
English	Sickle cell disease without crisis	A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may present with fatigue, shortness of breath, dizziness, headaches, pallor of skin or mucous membranes, and jaundice. This disorder is confirmed by identification of HbS mutation by genetic testing.