Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | age related macular degeneration 1 | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:22949395 more ... | Alzheimer's disease | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Alzheimer disease and early onset | ClinVar | PMID:10213549 more ... | Alzheimer's disease 2 | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10213549 more ... | Alzheimer's disease 3 | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10432380 more ... | Alzheimer's disease 4 | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10213152 more ... | Apolipoprotein E, Deficiency or Defect of | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Apolipoprotein e and deficiency or defect of | ClinVar | PMID:11500500 more ... | Broad-Betalipoproteinemia | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:11500500 more ... | Coumarin Sensitivity | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: COUMARIN SENSITIVITY | ClinVar | PMID:10213549 more ... | Dysbetalipoproteinemia due to Defect in Apolipoprotein E-d | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Dysbetalipoproteinemia due to defect in apolipoprotein e-d | ClinVar | PMID:11500500 more ... | Dyslipidemias | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Dyslipidemia | ClinVar | | Familial Hyperbeta- and Prebetalipoproteinemia | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Familial hyperbeta- and prebetalipoproteinemia | ClinVar | PMID:11500500 more ... | familial hypercholesterolemia | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Familial hypercholesterolemia | ClinVar | | Floating-Betalipoproteinemia | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Floating-betalipoproteinemia | ClinVar | PMID:11500500 more ... | genetic disease | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 more ... | Hypercholesterolemia | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:16103896 more ... | Hyperlipemia with Familial Hypercholesterolemic Xanthomatosis | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hyperlipemia with familial hypercholesterolemic xanthomatosis | ClinVar | PMID:11500500 more ... | hyperlipoproteinemia type III | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10587578 more ... | Lipoprotein Glomerulopathy | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Lipoprotein glomerulopathy | ClinVar | PMID:10213549 more ... | Presenile and Senile Dementia | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Presenile and senile dementia | ClinVar | PMID:10213549 more ... | sea-blue histiocytosis | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:22949395 more ... | warfarin resistance | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Coumarin resistance | ClinVar | PMID:10213549 more ... | warfarin sensitivity | | ISO | APOE (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Warfarin sensitivity | ClinVar | PMID:10213549 more ... | |