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Preferred Name

克兰费尔特综合征,核型47,XXY
ID

http://purl.bmicc.cn/ontology/ICD10CN/Q98.0
cui

C0022735
free_Translation

http://purl.bioontology.org/ontology/ICD10/Q98.0
has_exact_match

http://purl.bioontology.org/ontology/ICD10/Q98.0
hasDbXref

SNOMEDCT_US_2016_03_01:157021007

DOID:DOID_1921

SNOMEDCT_US_2016_03_01:268357008
hasSTY

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

Q98.0 克兰费尔特综合征,核型47,XXY
notation

Q98.0
prefixIRI

ICD10CN:Q98.0
prefLabel

克兰费尔特综合征,核型47,XXY
tui

T047
subClassOf

http://purl.bmicc.cn/ontology/ICD10CN/Q98
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http://purl.bioontology.org/ontology/ICD10/Q98.4 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
http://purl.bioontology.org/ontology/ICD10CM/Q98.4 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/MESH/D007713 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/ICD10/Q98.0 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU032889 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/ICD10CM/Q98.0 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/MEDLINEPLUS/C0022735 MedlinePlus Health Topics / MedlinePlus网站健康主题 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU028322 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI