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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 ..Bradycardia (D001919)
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:	1440
Name:	Bradycardia
Definition:	Cardiac arrhythmias that are characterized by excessively slow HEART RATE, usually below 50 beats per minute in human adults. They can be classified broadly into SINOATRIAL NODE dysfunction and ATRIOVENTRICULAR BLOCK.
Alternative IDs:
ParentIDs:	MESH:D001145
TreeNumbers:	C14.280.067.319 \|C23.550.073.300
Synonyms:	Bradyarrhythmia \|Bradyarrhythmias \|Bradycardias
Slim Mappings:	Cardiovascular disease\|Pathology (process)
Reference:	MedGen: D001919 MeSH: D001919 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants