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Preferred Name

β地中海贫血 / Beta thalassaemia
Definitions

Beta-thalassemia (BT) is a haemoglobinopathy characterised by deficiency (Beta+) or absence (Beta0) of synthesis of the beta globin chains of haemoglobin (Hb). Three main types of BT have been described: minor, intermedia and major with clinical presentation ranging from asymptomatic forms to microcytic anaemia and splenomegaly due to defective erythropiesis and haemolysis.
ID

http://purl.bmicc.cn/ontology/ICD11CN/3A50.2
definition

Beta-thalassemia (BT) is a haemoglobinopathy characterised by deficiency (Beta+) or absence (Beta0) of synthesis of the beta globin chains of haemoglobin (Hb). Three main types of BT have been described: minor, intermedia and major with clinical presentation ranging from asymptomatic forms to microcytic anaemia and splenomegaly due to defective erythropiesis and haemolysis.
hasDbXref

http://id.who.int/icd/release/11/2019-04/mms/2063292324
label

β地中海贫血 / Beta thalassaemia
mappingRelation

http://purl.bmicc.cn/ontology/ICD10CN/D56.1
notation

3A50.2
prefixIRI

ICD11CN:A50.2
prefLabel

β地中海贫血 / Beta thalassaemia
subClassOf

http://purl.bmicc.cn/ontology/ICD11CN/3A50
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http://purl.bioontology.org/ontology/ICD10/D56.1 International Classification of Diseases, Version 10 LOOM