Preferred Name

未特指的凝血缺陷

ID

http://purl.bmicc.cn/ontology/ICD10CN/D68.9

cui

C0005779

free_Translation

http://purl.bioontology.org/ontology/ICD10/D68.9

has_exact_match

http://purl.bioontology.org/ontology/ICD10/D68.9

hasDbXref

DOID:DOID_1247

hasSTY

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

label

D68.9 未特指的凝血缺陷

notation

D68.9

prefixIRI

ICD10CN:D68.9

prefLabel

未特指的凝血缺陷

tui

T047

subClassOf

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

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http://purl.bioontology.org/ontology/ICD10/D68.9 International Classification of Diseases, Version 10 CUI
http://purl.bioontology.org/ontology/ICD10CM/D68.9 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/OMIM/MTHU033936 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0005779 MedlinePlus Health Topics CUI
http://purl.bioontology.org/ontology/OMIM/MTHU008649 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/MESH/D001778 Medical Subject Headings CUI