Jump to:
Spinner 000000 16px loading...
Preferred Name

Supravalvular aortic stenosis
ID

http://purl.bioontology.org/ontology/ICD10CM/Q25.3
cui

C0003499
EXCLUDES1

congenital aortic stenosis NOS (Q23.0); congenital stenosis of aortic valve (Q23.0)
notation

Q25.3
Order number

28963
prefLabel

Supravalvular aortic stenosis
tui

T047
subClassOf

http://purl.bioontology.org/ontology/ICD10CM/Q25
Add comment
Add proposal
Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/MTHU014953 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU014953 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bioontology.org/ontology/MESH/D021921 Medical Subject Headings / 医学主题词表 CUI
http://purl.obolibrary.org/obo/DOID_1929 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_1929 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0008504 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0008504 Experimental Factor Ontology / 实验性因素本体 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C85176 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.bioontology.org/ontology/OMIM/185500 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/185500 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.obolibrary.org/obo/HP_0004381 Human Phenotype Ontology / 人类表型本体 LOOM
http://www.orpha.net/ORDO/Orphanet_3193 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.bioontology.org/ontology/OMIM/130160 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI