Preferred Name

血管炎 / Vasculitis

Definitions

Vasculitides represent a heterogenous group of diseases of multifactorial aetiology characterized by inflammatory lesions of vessels. These lesions consist of fibrinoid necrosis (necrotizing arteritis), giant cell infiltration without necrosis, immunoglobulins deposit or leukocytoclastic infiltration. The spectrum and severity of the systemic vaculitides is broad, from life or sight threatening fulminant disease to relatively minor skin disease.

ID

http://purl.bmicc.cn/ontology/ICD11CN/4A44

Coded_Elsewhere

Thrombotic microangiopathy, not elsewhere classified (3B65)

Behçet disease (4A62)

definition

Vasculitides represent a heterogenous group of diseases of multifactorial aetiology characterized by inflammatory lesions of vessels. These lesions consist of fibrinoid necrosis (necrotizing arteritis), giant cell infiltration without necrosis, immunoglobulins deposit or leukocytoclastic infiltration. The spectrum and severity of the systemic vaculitides is broad, from life or sight threatening fulminant disease to relatively minor skin disease.

hasDbXref

http://id.who.int/icd/release/11/2019-04/mms/572581721

label

血管炎 / Vasculitis

mappingRelation

http://purl.bmicc.cn/ontology/ICD10CN/M30-M36

notation

4A44

note

requiredPCNote

prefixIRI

ICD11CN:A44

prefLabel

血管炎 / Vasculitis

subClassOf

http://purl.bmicc.cn/ontology/ICD11CN/L1-4A4

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http://purl.obolibrary.org/obo/SYMP_0000153 Human Disease Ontology 123 LOOM
http://purl.obolibrary.org/obo/HP_0002633 Human Phenotype Ontology LOOM
http://purl.bioontology.org/ontology/MESH/D014657 Medical Subject Headings LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU018875 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/LNC/LA17783-4 Logical Observation Identifier Names and Codes LOOM
http://purl.obolibrary.org/obo/MPATH_201 Human Phenotype Ontology China LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26912 National Cancer Institute Thesaurus LOOM
http://purl.obolibrary.org/obo/DOID_865 Human Disease Ontology 123 LOOM