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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Coronary Disease (D003327)
..Starting node ..Coronary Vasospasm (D003329)
Child Nodes:
........Hypertension Resistant to Conventional Therapy (C563514)
Sister Nodes:
..Coronary Aneurysm (D003323)
..Coronary Artery Disease (D003324) 4
..Coronary Occlusion (D054059)
..Coronary Stenosis (D023921) 1
..Coronary Thrombosis (D003328)
..Coronary Vasospasm (D003329) 1
..Coronary-Subclavian Steal Syndrome (D058686)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	2767
Name:	Coronary Vasospasm
Definition:	Spasm of the large- or medium-sized coronary arteries.
Alternative IDs:
ParentIDs:	MESH:D003327
TreeNumbers:	C14.280.647.250.295 \|C14.907.585.250.295
Synonyms:	Artery Vasospasm, Coronary \|Artery Vasospasms, Coronary \|Coronary Artery Vasospasm \|Coronary Artery Vasospasms \|Coronary Vasospasms \|Vasospasm, Coronary \|Vasospasm, Coronary Artery \|Vasospasms, Coronary \|Vasospasms, Coronary Artery
Slim Mappings:	Cardiovascular disease
Reference:	MedGen: D003329 MeSH: D003329 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants