International Classification of Diseases, 10th Edition, China

Last uploaded: November 11, 2019

Preferred Name	遗传性因子Ⅶ缺乏
ID	http://purl.bmicc.cn/ontology/ICD10CN/D66
cui	C0019069
free_Translation	http://purl.bioontology.org/ontology/ICD10/D66
has_exact_match	http://purl.bioontology.org/ontology/ICD10/D66
hasDbXref	SNOMEDCT_US_2016_03_01:28293008 UMLS_CUI:C0019069 OMIM:134500 ICD9CM:286.0 NCI:C27146 MESH:D006467 DOID:DOID_12134
hasSTY	http://purl.bioontology.org/ontology/STY/T047
label	D66 遗传性因子Ⅶ缺乏
notation	D66
prefixIRI	ICD10CN:D66
prefLabel	遗传性因子Ⅶ缺乏
tui	T047
subClassOf	http://purl.bmicc.cn/ontology/ICD10CN/D65-D69.9

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/OMIM/300841	Online Mendelian Inheritance in Man	CUI
http://purl.bioontology.org/ontology/OMIM/306700	Online Mendelian Inheritance in Man	CUI
http://purl.bioontology.org/ontology/ICD10CM/D66	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.bioontology.org/ontology/MESH/D006467	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/ICD10/D66	International Classification of Diseases, Version 10	CUI