Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | arrhythmogenic right ventricular cardiomyopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:16199547 more ... | arrhythmogenic right ventricular dysplasia 9 | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Arrhythmogenic right ventricular dysplasia 9 | ClinVar | PMID:25741868 and PMID:28492532 | atrial heart septal defect | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Atrial septal defect | ClinVar | PMID:23861362 more ... | atrial heart septal defect 3 | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Atrial septal defect 3 | ClinVar | PMID:11815426 more ... | atrioventricular block | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: AV Block Third Degree Adverse Event | ClinVar | PMID:17576681 more ... | autosomal dominant hyaline body myopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Congenital myopathy 7A more ... | ClinVar | | Brain-Lung-Thyroid Syndrome | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Brain-lung-thyroid syndrome | ClinVar | PMID:25741868 | Brugada syndrome | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Sudden Unexplained Nocturnal Death Syndrome (SUNDS) | ClinVar | PMID:23861362 more ... | cardiac arrest | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cardiac arrest | ClinVar | PMID:25741868 and PMID:28492532 | cardiomyopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:15998695 more ... | cardiomyopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:15998695 more ... | congenital heart disease | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Heart and malformation of | ClinVar | PMID:16199547 more ... | congestive heart failure | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:20656787 more ... | dilated cardiomyopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:15998695 more ... | dilated cardiomyopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:15998695 more ... | dilated cardiomyopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:15998695 more ... | dilated cardiomyopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:15998695 more ... | dilated cardiomyopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:15998695 more ... | dilated cardiomyopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:15998695 more ... | dilated cardiomyopathy 1A | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Dilated cardiomyopathy 1A | ClinVar | PMID:24033266 more ... | dilated cardiomyopathy 1B | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hypokinetic dilated cardiomyopathy and familial | ClinVar | PMID:15998695 more ... | dilated cardiomyopathy 1EE | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Dilated cardiomyopathy 1EE | ClinVar | PMID:11815426 more ... | dilated cardiomyopathy 1H | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Dilated cardiomyopathy with conduction defect | ClinVar | PMID:24033266 more ... | Dilated Cardiomyopathy with Left Ventricular Noncompaction | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Left ventricular noncompaction cardiomyopathy | ClinVar | PMID:23861362 more ... | distal myopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | | distal myopathy 1 | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | | familial hypertrophic cardiomyopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:15998695 more ... | familial hypertrophic cardiomyopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:15998695 more ... | familial hypertrophic cardiomyopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:15998695 more ... | genetic disease | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:20656787 more ... | Heart Block | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Conduction disorder of the heart | ClinVar | PMID:25741868 | heart disease | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Heart disease | ClinVar | PMID:23861362 more ... | hemiplegia | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hemiplegia | ClinVar | PMID:15998695 more ... | hyaline body myopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Myosin storage myopathy | ClinVar | | hypertrophic cardiomyopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hypertrophic cardiomyopathy | ClinVar | PMID:15998695 more ... | hypertrophic cardiomyopathy 1 | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11815426 more ... | hypertrophic cardiomyopathy 1 | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11815426 more ... | hypertrophic cardiomyopathy 1 | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11815426 more ... | hypertrophic cardiomyopathy 14 | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11815426 more ... | hypoplastic left heart syndrome | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hypoplastic left heart syndrome | ClinVar | PMID:25741868 | left ventricular noncompaction | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Left ventricular noncompaction | ClinVar | PMID:24033266 more ... | Left Ventricular Noncompaction 1 | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Left ventricular noncompaction 1 | ClinVar | PMID:24120998 more ... | long QT syndrome | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 and PMID:28492532 | long QT syndrome | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:23861362 more ... | lysinuric protein intolerance | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Lysinuric protein intolerance | ClinVar | PMID:28492532 | migraine | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Migraine Disorders | ClinVar | PMID:15998695 more ... | restrictive cardiomyopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Restrictive cardiomyopathy | ClinVar | PMID:23861362 more ... | scapuloperoneal myopathy | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Scapuloperoneal myopathy | ClinVar | | Sick Sinus Syndrome 3 | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Sick sinus syndrome 3 and susceptibility to | ClinVar | PMID:11815426 more ... | Specific Granule Deficiency | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Specific granule deficiency | ClinVar | PMID:11313242 more ... | Sudden Cardiac Death | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Sudden cardiac death | ClinVar | PMID:15998695 more ... | Sudden Unexpected Nocturnal Death Syndrome | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Sudden unexpected nocturnal death syndrome | ClinVar | PMID:23861362 more ... | Ventricular Fibrillation | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Ventricular fibrillation | ClinVar | PMID:25741868 more ... | Ventricular Tachycardia | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Ventricular tachycardia | ClinVar | PMID:15998695 more ... | Wolff-Parkinson-White syndrome | | ISO | MYH6 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Wolff-Parkinson-White pattern | ClinVar | PMID:15998695 more ... | |