International Classification of Diseases, 11th Edition, China

Last uploaded: November 11, 2019

Preferred Name	免疫性血小板减少性紫癜 / Immune thrombocytopenic purpura
Definitions	Immune thrombocytopenic purpura (or immune thrombocytopenia; ITP) is an autoimmune coagulation disorder characterised by isolated thrombocytopenia (a platelet count <100,000/microL), in the absence of any underlying disorder that may be associated with thrombocytopenia.
ID	http://purl.bmicc.cn/ontology/ICD11CN/3B64.10
Coded_Elsewhere	Evans syndrome (3A20.5)
definition	Immune thrombocytopenic purpura (or immune thrombocytopenia; ITP) is an autoimmune coagulation disorder characterised by isolated thrombocytopenia (a platelet count <100,000/microL), in the absence of any underlying disorder that may be associated with thrombocytopenia.
hasDbXref	http://id.who.int/icd/release/11/2019-04/mms/364346400
label	免疫性血小板减少性紫癜 / Immune thrombocytopenic purpura
mappingRelation	http://purl.bmicc.cn/ontology/ICD10CN/D69.3
notation	3B64.10
prefixIRI	ICD11CN:B64.10
prefLabel	免疫性血小板减少性紫癜 / Immune thrombocytopenic purpura
subClassOf	http://purl.bmicc.cn/ontology/ICD11CN/3B64.1

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	http://purl.bioontology.org/ontology/ICD10CM/D69.3	International Classification of Diseases, Version 10 - Clinical Modification	LOOM