Preferred Name |
镰状细胞病不伴象 / Sickle cell disease without crisis |
Definitions |
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. |
ID |
http://purl.bmicc.cn/ontology/ICD11CN/3A51.1 |
definition |
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. |
hasDbXref | |
label |
镰状细胞病不伴象 / Sickle cell disease without crisis |
mappingRelation | |
notation |
3A51.1 |
prefixIRI |
ICD11CN:A51.1 |
prefLabel |
镰状细胞病不伴象 / Sickle cell disease without crisis |
subClassOf |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.bioontology.org/ontology/ICD10CM/D57.1 | International Classification of Diseases, Version 10 - Clinical Modification | LOOM |