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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: Tachycardia (D013610)
..Starting node ..Tachycardia, Supraventricular (D013617)
Child Nodes:
........Tachycardia, Ectopic Atrial (D013612)
........Tachycardia, Ectopic Junctional (D013613)
........Tachycardia, Sinus (D013616)
Sister Nodes:
..Atrial Tachyarrhythmia with Short PR Interval (C566237)
..Bidirectional tachycardia (C535438)
..Tachycardia, Hypertension, Microphthalmia, And Hyperglycinuria (C566880)
..Tachycardia, Paroxysmal (D013614) 1
..Tachycardia, Reciprocating (D054139) 2
..Tachycardia, Supraventricular (D013617) 3
..Tachycardia, Ventricular (D017180) 7
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	10859
Name:	Tachycardia, Supraventricular
Definition:	A generic expression for any tachycardia that originates above the BUNDLE OF HIS.
Alternative IDs:
ParentIDs:	MESH:D013610
TreeNumbers:	C14.280.067.845.880 \|C23.550.073.845.880
Synonyms:	Supraventricular Tachycardia \|Supraventricular Tachycardias \|Tachycardias, Supraventricular
Slim Mappings:	Cardiovascular disease\|Pathology (process)
Reference:	MedGen: D013617 MeSH: D013617 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants