溶血尿毒症综合征 / Haemolytic uraemic syndrome

A disease caused by acquired haematopoietic stem cell mutation defect of the PIGA gene in the X chromosome leading to the premature break down of red blood cells. This disease is characterised by haemolytic anaemia, thrombosis and. This disease may present with haemoglobinuria (blood in the urine will be most noticeable in the morning, and clear as the day progresses), pallor, fatigue, or shortness of breath. Confirmation is by identification of genetic mutation in the PIGA gene through genetic testing.

http://purl.bmicc.cn/ontology/ICD11CN/3A21.2

A disease caused by acquired haematopoietic stem cell mutation defect of the PIGA gene in the X chromosome leading to the premature break down of red blood cells. This disease is characterised by haemolytic anaemia, thrombosis and. This disease may present with haemoglobinuria (blood in the urine will be most noticeable in the morning, and clear as the day progresses), pallor, fatigue, or shortness of breath. Confirmation is by identification of genetic mutation in the PIGA gene through genetic testing.

Hereditary haemolytic uraemic syndrome (3A10)

http://id.who.int/icd/release/11/2019-04/mms/630790515

溶血尿毒症综合征 / Haemolytic uraemic syndrome

http://purl.bmicc.cn/ontology/ICD10CN/D59.3

3A21.2

ICD11CN:A21.2

溶血尿毒症综合征 / Haemolytic uraemic syndrome

http://purl.bmicc.cn/ontology/ICD11CN/3A21