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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 ..Cardiac Conduction Defect, Nonprogressive (C566186)
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:	1688
Name:	Cardiac Conduction Defect, Nonprogressive
Definition:
Alternative IDs:
ParentIDs:	MESH:D001145
TreeNumbers:	C14.280.067/C566186 \|C23.550.073/C566186
Synonyms:
Slim Mappings:	Cardiovascular disease\|Pathology (process)
Reference:	MedGen: C566186 MeSH: C566186 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants