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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 ..Adams-Stokes Syndrome (D000219)
Child Nodes:
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:	255
Name:	Adams-Stokes Syndrome
Definition:	A condition of fainting spells caused by heart block, often an atrioventricular block, that leads to BRADYCARDIA and drop in CARDIAC OUTPUT. When the cardiac output becomes too low, the patient faints (SYNCOPE). In some cases, the syncope attacks are transient and in others cases repetitive and persistent.
Alternative IDs:
ParentIDs:	MESH:D006327
TreeNumbers:	C14.280.067.558.137 \|C23.550.073.425.025
Synonyms:	Adams Stokes Syndrome \|Adam Stokes Attacks \|Adam-Stokes Attacks \|Attacks, Adam-Stokes \|Attacks, Stokes-Adams \|Stokes Adams Attacks \|Stokes-Adams Attacks \|Stokes Adams Syndrome \|Stokes-Adams Syndrome \|Syndrome, Adams-Stokes \|Syndrome, Stokes-Adams
Slim Mappings:	Cardiovascular disease\|Pathology (process)
Reference:	MedGen: D000219 MeSH: D000219 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants