Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | atrial fibrillation | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Atrial fibrillation | ClinVar | | cardiomyopathy | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cardiomyopathy | ClinVar | | Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: DiGeorge syndrome/velocardiofacial syndrome complex 2 | ClinVar | PMID:24033266 more ... | dilated cardiomyopathy | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11140941 more ... | dilated cardiomyopathy | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11140941 more ... | dilated cardiomyopathy | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11140941 more ... | dilated cardiomyopathy | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11140941 more ... | dilated cardiomyopathy | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11140941 more ... | dilated cardiomyopathy | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11140941 more ... | familial hypertrophic cardiomyopathy | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Primary familial hypertrophic cardiomyopathy | ClinVar | PMID:24033266 more ... | genetic disease | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:24033266 more ... | hypertrophic cardiomyopathy | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hypertrophic cardiomyopathy | ClinVar | PMID:20951326 more ... | hypertrophic cardiomyopathy 1 | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Idiopathic hypertrophic subaortic stenosis | ClinVar | PMID:24033266 more ... | long QT syndrome | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:24033266 more ... | Sudden Cardiac Death | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Sudden cardiac death | ClinVar | | Sudden Death | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Sudden unexplained death | ClinVar | PMID:24033266 more ... | Wolff-Parkinson-White syndrome | | ISO | NEBL (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Wolff-Parkinson-White pattern | ClinVar | | | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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