Preferred Name

其他凝血因子的遗传性缺乏

ID

http://purl.bmicc.cn/ontology/ICD10CN/D68.2

cui

C0494242

free_Translation

http://purl.bioontology.org/ontology/ICD10/D68.2

has_exact_match

http://purl.bioontology.org/ontology/ICD10/D68.2

hasDbXref

DOID:DOID_2236

DOID:DOID_2215

DOID:DOID_2216

hasSTY

http://purl.bioontology.org/ontology/STY/T047

label

D68.2 其他凝血因子的遗传性缺乏

notation

D68.2

prefixIRI

ICD10CN:D68.2

prefLabel

其他凝血因子的遗传性缺乏

tui

T047

subClassOf

http://purl.bmicc.cn/ontology/ICD10CN/D68

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http://purl.bioontology.org/ontology/ICD10/D68.2 International Classification of Diseases, Version 10 CUI
http://purl.bioontology.org/ontology/ICD10CM/D68.2 International Classification of Diseases, Version 10 - Clinical Modification CUI