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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: Arrhythmias, Cardiac (D001145)
..Starting node ..Parasystole (D017574)
Child Nodes:
Sister Nodes:
..Arrhythmia, Sinus (D001146) 5
..Atrial Fibrillation (D001281) 8
..Atrial Flutter (D001282)
..Atrial Septal Defect, Secundum, with Various Cardiac and Noncardiac Defects (C566351)
..Bradycardia (D001919)
..Brugada Syndrome (D053840) 9
..Cardiac Arrhythmia, Ankyrin-B-Related (C566996)
..Cardiac Complexes, Premature (D005117) 4
..Cardiac Conduction Defect (C562490)
..Cardiac Conduction Defect, Nonprogressive (C566186)
..Commotio Cordis (D056104)
..Heart Block (D006327) 19
..Long QT Syndrome (D008133) 20
..Parasystole (D017574)
..Pre-Excitation Syndromes (D011226) 3
..QT INTERVAL, VARIATION IN (OMIM:610141)
..Short Qt Syndrome (C580439)
..Short QT Syndrome 1 (C566506)
..Short QT Syndrome 2 (C566505)
..Short QT Syndrome 3 (C566504)
..Simpson-Golabi-Behmel syndrome (C537340)
..Tachycardia (D013610) 20
..Ventricular Fibrillation (D014693) 3
..Ventricular Flutter (D054141)
..Woodhouse Sakati syndrome (C536742)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8632
Name:	Parasystole
Definition:	A cardiac arrhythmia that is caused by interaction of two independently initiated cardiac impulses of different rates from two separate foci. Generally one focus is the SINOATRIAL NODE, the normal pacemaker. The ectopic focus is usually in the HEART VENTRICLE but can be in the HEART ATRIUM or the ATRIOVENTRICULAR NODE. Modulation of the parasystolic rhythm by the sinus rhythm depends on the completeness of entrance block surrounding the parasystolic focus.
Alternative IDs:
ParentIDs:	MESH:D001145
TreeNumbers:	C14.280.067.672 \|C23.550.073.670
Synonyms:	Parasystoles
Slim Mappings:	Cardiovascular disease\|Pathology (process)
Reference:	MedGen: D017574 MeSH: D017574 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants