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Preferred Name

Von Willebrand disease
ID

http://purl.bioontology.org/ontology/ICD10CM/D68.0
cui

C0042974
EXCLUDES1

capillary fragility (hereditary) (D69.8); factor VIII deficiency NOS (D66); factor VIII deficiency with functional defect (D66)
notation

D68.0
Order number

03555
prefLabel

Von Willebrand disease
tui

T047
subClassOf

http://purl.bioontology.org/ontology/ICD10CM/D68
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http://purl.bmicc.cn/ontology/ICD10CN/D68.0 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI
http://www.orpha.net/ORDO/Orphanet_903 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://www.orpha.net/ORDO/Orphanet_903 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bioontology.org/ontology/MESH/D014842 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/ICD10/D68.0 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C68677 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0042974 MedlinePlus Health Topics / MedlinePlus网站健康主题 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU016680 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU016680 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM