镰状细胞疾患或其他血红蛋白病 / Sickle cell disorders or other haemoglobinopathies

Any 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.

http://purl.bmicc.cn/ontology/ICD11CN/3A51

Any 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.

http://id.who.int/icd/release/11/2019-04/mms/975559344

镰状细胞疾患或其他血红蛋白病 / Sickle cell disorders or other haemoglobinopathies

http://purl.bmicc.cn/ontology/ICD10CN/D57

3A51

ICD11CN:A51

镰状细胞疾患或其他血红蛋白病 / Sickle cell disorders or other haemoglobinopathies

http://purl.bmicc.cn/ontology/ICD11CN/L1-3A0