Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | achromatopsia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia | ClinVar | PMID:16199547 more ... | achromatopsia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia | ClinVar | PMID:24033266 | achromatopsia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia | ClinVar | PMID:28041643 | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:26029869 | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:25741868 more ... | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:26029869 more ... | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:25741868 | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:25741868 and PMID:28492532 | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:25741868 and PMID:28492532 | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:25741868 and PMID:28492532 | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:25741868 and PMID:28492532 | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:25741868 and PMID:28492532 | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:25741868 and PMID:28492532 | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:26029869 | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:26029869 | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:26029869 | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:26029869 | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:26029869 | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:26029869 | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:26063662 | achromatopsia 7 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Achromatopsia 7 | ClinVar | PMID:24824130 and PMID:26063662 | autoimmune interstitial lung, joint, and kidney disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Autoimmune interstitial lung more ... | ClinVar | PMID:28492532 | Charcot-Marie-Tooth disease type 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Charcot-Marie-Tooth disease and type I | ClinVar | PMID:28492532 | gastrointestinal stromal tumor | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Gastrointestinal stromal tumor | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | macular degeneration | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Macular dystrophy | ClinVar | PMID:28041643 | parathyroid carcinoma | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Parathyroid carcinoma | ClinVar | PMID:28492532 | 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