《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China

Last uploaded: November 11, 2019

Preferred Name	家族性自主神经功能异常[赖利-戴]
ID	http://purl.bmicc.cn/ontology/ICD10CN/G90.1
cui	C0013364
free_Translation	http://purl.bioontology.org/ontology/ICD10/G90.1
has_exact_match	http://purl.bioontology.org/ontology/ICD10/G90.1
hasDbXref	NCI:C84706 SNOMEDCT_US_2016_03_01:204087006 OMIM:223900 DOID:DOID_11589 MESH:D004402 UMLS_CUI:C0013364 SNOMEDCT_US_2016_03_01:29159009
hasSTY	http://purl.bioontology.org/ontology/STY/T047 http://purl.bioontology.org/ontology/STY/T019
label	G90.1 家族性自主神经功能异常[赖利-戴]
notation	G90.1
prefixIRI	ICD10CN:G90.1
prefLabel	家族性自主神经功能异常[赖利-戴]
tui	T019 T047
subClassOf	http://purl.bmicc.cn/ontology/ICD10CN/G90

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MESH/D004402	Medical Subject Headings / 医学主题词表	CUI
http://purl.bioontology.org/ontology/ICD10/G90.1	International Classification of Diseases, Version 10 / 《国际疾病分类》第10版	CUI
http://purl.bioontology.org/ontology/ICD10CM/G90.1	International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改	CUI
http://purl.bioontology.org/ontology/OMIM/223900	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	CUI
http://purl.bioontology.org/ontology/OMIM/603722	Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库	CUI