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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 Diseases (D006331)
..Starting node ..Heart Rupture (D006341)
Child Nodes:
........Heart Rupture, Post-Infarction (D006342) 1
Sister Nodes:
..Arrhythmias, Cardiac (D001145) 112
..Carcinoid Heart Disease (D002275)
..Cardiac Output, High (D016534)
..Cardiac Output, Low (D002303)
..Cardiac Tamponade (D002305)
..Cardiomegaly (D006332) 46
..Cardiomyopathies (D009202) 124
..Endocarditis (D004696) 3
..Gangliosidosis, Generalized GM1, Type I, with Cardiac Involvement (C566895)
..Glycogen Storage Disease of Heart, Lethal Congenital (C564888)
..Heart Aneurysm (D006322)
..Heart Arrest (D006323) 3
..Heart Defects, Congenital (D006330) 285
..Heart Failure (D006333) 5
..Heart Neoplasms (D006338) 3
..Heart Rupture (D006341) 2
..Heart Valve Diseases (D006349) 76
..Myocardial Ischemia (D017202) 28
..Pericardial Effusion (D010490) 1
..Pericarditis (D010493) 3
..Pneumopericardium (D011026)
..Postpericardiotomy Syndrome (D011185)
..Pulmonary Heart Disease (D011660)
..Rheumatic Heart Disease (D012214)
..Ventricular Dysfunction (D018754) 4
..Ventricular Outflow Obstruction (D014694) 44
..Yorifuji Okuno syndrome (C536714)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4950
Name:	Heart Rupture
Definition:	Disease-related laceration or tearing of tissues of the heart, including the free-wall MYOCARDIUM; HEART SEPTUM; PAPILLARY MUSCLES; CHORDAE TENDINEAE; and any of the HEART VALVES. Pathological rupture usually results from myocardial infarction (HEART RUPTURE, POST-INFARCTION).
Alternative IDs:
ParentIDs:	MESH:D006331
TreeNumbers:	C14.280.470
Synonyms:	Cardiac Free Wall Rupture \|Cardiac Rupture \|Cardiac Ruptures \|Free Wall Rupture, Heart \|Heart Ruptures \|Ventricular Free Wall Rupture
Slim Mappings:	Cardiovascular disease
Reference:	MedGen: D006341 MeSH: D006341 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants