Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Alzheimer's disease | | ISO | APP (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10097173 more ... | Alzheimer's disease 1 | | ISO | APP (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10097173 more ... | Alzheimer's Disease, Early-Onset, with Cerebral Amyloid Angiopathy | | ISO | APP (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Alzheimer disease more ... | ClinVar | PMID:16369530 and PMID:19047566 | APP-related cerebral amyloid angiopathy | | ISO | APP (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10441572 more ... | CST3-related cerebral amyloid angiopathy | | ISO | APP (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary cerebral hemorrhage with amyloidosis | ClinVar | PMID:25604855 more ... | familial focal epilepsy with variable foci | | ISO | APP (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Familial focal epilepsy with variable foci | ClinVar | PMID:25741868 | genetic disease | | ISO | APP (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | Neurodevelopmental Disorders | | ISO | APP (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Neurodevelopmental disorder | ClinVar | PMID:25741868 | Presenile and Senile Dementia | | ISO | APP (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Presenile and senile dementia | ClinVar | PMID:10821838 more ... | vascular dementia | | ISO | APP (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Vascular dementia | ClinVar | PMID:22312439 more ... | |