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

http://id.who.int/icd/release/11/2019-04/mms/1711513381

label

镰状细胞病不伴象 / Sickle cell disease without crisis

mappingRelation

http://purl.bmicc.cn/ontology/ICD10CN/D57.1

notation

3A51.1

prefixIRI

ICD11CN:A51.1

prefLabel

镰状细胞病不伴象 / Sickle cell disease without crisis

subClassOf

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

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http://purl.bioontology.org/ontology/ICD10CM/D57.1 International Classification of Diseases, Version 10 - Clinical Modification LOOM