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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 ..Sinoatrial Block (D012848)
Child Nodes:
........Mental retardation, keratoconus, febrile seizures, and sinoatrial block (C537452)
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:	10252
Name:	Sinoatrial Block
Definition:	Disturbance in the atrial activation that is caused by transient failure of impulse conduction from the SINOATRIAL NODE to the HEART ATRIA. It is characterized by a delayed in heartbeat and pauses between P waves in an ELECTROCARDIOGRAM.
Alternative IDs:
ParentIDs:	MESH:D006327
TreeNumbers:	C14.280.067.558.750 \|C23.550.073.425.780
Synonyms:	Block, Sinoatrial \|Block, Sinoatrial Exit \|Blocks, Sinoatrial \|Blocks, Sinoatrial Exit \|Exit Block, Sinoatrial \|Exit Blocks, Sinoatrial \|Sinoatrial Blocks \|Sinoatrial Exit Block \|Sinoatrial Exit Blocks
Slim Mappings:	Cardiovascular disease\|Pathology (process)
Reference:	MedGen: D012848 MeSH: D012848 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants