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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: Heart Block (D006327)
..Starting node ..Bundle-Branch Block (D002037)
Child Nodes:
........Bundle Branch Block, Familial Isolated Complete Right (C562759)
Sister Nodes:
..Adams-Stokes Syndrome (D000219)
..Atrial Septal Defect with Atrioventricular Conduction Defects (C566238) 1
..Atrial Standstill (C563984)
..Atrioventricular Block (D054537) 1
..Bundle-Branch Block (D002037) 1
..Congenital heart block (C535758) 1
..Heart Block, Nonprogressive (C566185)
..Hereditary bundle branch system defect (C566873)
..Progressive Familial Heart Block, Type Ib (C567037)
..Progressive Familial Heart Block, Type II (C564202)
..Sick Sinus Syndrome (D012804) 3
..Sinoatrial Block (D012848) 1
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1534
Name:	Bundle-Branch Block
Definition:	A form of heart block in which the electrical stimulation of HEART VENTRICLES is interrupted at either one of the branches of BUNDLE OF HIS thus preventing the simultaneous depolarization of the two ventricles.
Alternative IDs:
ParentIDs:	MESH:D006327
TreeNumbers:	C14.280.067.558.323 \|C23.550.073.425.100
Synonyms:	Anterior Fascicular Block \|Anterior Fascicular Blocks \|Block, Anterior Fascicular \|Block, Bundle Branch \|Block, Bundle-Branch \|Block, Fascicular \|Block, Left Bundle-Branch \|Block, Posterior Fascicular \|Block, Right Bundle-Branch \|Blocks, Anterior Fascicular \|Block
Slim Mappings:	Cardiovascular disease\|Pathology (process)
Reference:	MedGen: D002037 MeSH: D002037 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants