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Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | HAMP | Human | Brugada syndrome 5 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Brugada syndrome 5 | ClinVar | PMID:28492532 | HAMP | Human | dystonia | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Dystonic disorder | ClinVar | PMID:32581362 | HAMP | Human | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | HAMP | Human | genetic disease | | IAGP | RGD:155915691|RGD:401887174|RGD:597690221 | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | HAMP | Human | genetic disease | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 | HAMP | Human | hemochromatosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary hemochromatosis | ClinVar | PMID:14670915|PMID:16141345|PMID:19787796|PMID:21411349|PMID:25741868|PMID:26547814|PMID:28492532 | HAMP | Human | hemochromatosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary hemochromatosis | ClinVar | PMID:15198949|PMID:25741868|PMID:27007796|PMID:28492532 | HAMP | Human | hemochromatosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary hemochromatosis | ClinVar | PMID:16141345|PMID:18809758|PMID:28492532 | HAMP | Human | hemochromatosis | | IAGP | RGD:10042407|RGD:10405572|RGD:10405642|RGD:127232151|RGD:127256329|RGD:127309649|RGD:127315612|RGD:12887397|RGD:14715852|RGD:15142511|RGD:15169486|RGD:151881133|RGD:151893440|RGD:152062299|RGD:152109479|RGD:152130260|RGD:156058442|RGD:28907193|RGD:329352245|RGD:402464162|RGD:402475270|RGD:405105342|RGD:405105834|RGD:405106216|RGD:405106589|RGD:405106958|RGD:405109048|RGD:405109861|RGD:405109867|RGD:405109917|RGD:405109965|RGD:405110351|RGD:405110407|RGD:405114146|RGD:405114578|RGD:405114907|RGD:405115255|RGD:405116034|RGD:405116288|RGD:405176171|RGD:405176800|RGD:405177654|RGD:405178877|RGD:405183724|RGD:405186031|RGD:405187655|RGD:405189537|RGD:405197816|RGD:405199552|RGD:405215711|RGD:405239445|RGD:405239554|RGD:405250568|RGD:405253124|RGD:597901366|RGD:597904438 | 8554872 | ClinVar Annotator: match by term: Hereditary hemochromatosis | ClinVar | PMID:28492532 | HAMP | Human | hemochromatosis | | IAGP | RGD:127281811|RGD:127296867|RGD:28881147 | 8554872 | ClinVar Annotator: match by term: Hereditary hemochromatosis | ClinVar | PMID:25741868|PMID:28492532 | HAMP | Human | hemochromatosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary hemochromatosis | ClinVar | PMID:14630809|PMID:15024747|PMID:28492532 | HAMP | Human | hemochromatosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary hemochromatosis | ClinVar | PMID:17576681|PMID:28492532|PMID:9536098 | HAMP | Human | hemochromatosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary hemochromatosis | ClinVar | PMID:15099344|PMID:26310624|PMID:26799139|PMID:28492532 | HAMP | Human | hemochromatosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary hemochromatosis | ClinVar | PMID:15099344|PMID:22297252|PMID:22924847|PMID:28492532|PMID:33016646 | HAMP | Human | hemochromatosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary hemochromatosis | ClinVar | PMID:15082576|PMID:25741868|PMID:28492532 | HAMP | Human | hemochromatosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary hemochromatosis | ClinVar | PMID:12915468|PMID:21088809|PMID:25741868|PMID:28492532 | HAMP | Human | hemochromatosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hemochromatosis, juvenile, digenic | ClinVar | PMID:12915468 | HAMP | Human | hemochromatosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary hemochromatosis | ClinVar | PMID:12915468|PMID:19214511|PMID:28492532 | HAMP | Human | hemochromatosis | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary hemochromatosis | ClinVar | PMID:16199547|PMID:25741868|PMID:28492532 | HAMP | Human | hemochromatosis type 1 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hemochromatosis type 1 | ClinVar | PMID:12915468|PMID:19214511|PMID:28492532 | HAMP | Human | hemochromatosis type 2 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Juvenile hemochromatosis | ClinVar | | HAMP | Human | hemochromatosis type 2A | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hemochromatosis, type 2a, modifier of | ClinVar | PMID:12915468|PMID:19214511|PMID:28492532 | HAMP | Human | hemochromatosis type 2B | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hemochromatosis type 2B | ClinVar | PMID:14670915|PMID:16141345|PMID:19787796|PMID:21411349|PMID:25741868|PMID:26547814|PMID:28492532 | HAMP | Human | hemochromatosis type 2B | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hemochromatosis type 2B | ClinVar | PMID:15198949|PMID:25741868|PMID:27007796|PMID:28492532 | HAMP | Human | hemochromatosis type 2B | | IAGP | RGD:28907190|RGD:596925553 | 8554872 | ClinVar Annotator: match by term: Hemochromatosis type 2B | ClinVar | PMID:25741868 | HAMP | Human | hemochromatosis type 2B | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hemochromatosis type 2B | ClinVar | PMID:12915468|PMID:19214511|PMID:28492532 | HAMP | Human | hemochromatosis type 2B | | IAGP | RGD:12887397|RGD:28907193 | 8554872 | ClinVar Annotator: match by term: Hemochromatosis type 2B | ClinVar | PMID:28492532 | HAMP | Human | hemochromatosis type 2B | | IAGP | RGD:127296867|RGD:28881147 | 8554872 | ClinVar Annotator: match by term: Hemochromatosis type 2B | ClinVar | PMID:25741868|PMID:28492532 | HAMP | Human | hemochromatosis type 2B | | IAGP | RGD:8557984|RGD:8596374 | 8554872 | ClinVar Annotator: match by term: Hemochromatosis type 2B | ClinVar | PMID:12469120 | HAMP | Human | hemochromatosis type 2B | | IAGP | RGD:11623281|RGD:28907195|RGD:38457497 | 8554872 | ClinVar Annotator: match by term: Hemochromatosis type 2B | ClinVar | | HAMP | Human | hemochromatosis type 2B | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hemochromatosis type 2B | ClinVar | PMID:15099344|PMID:22297252|PMID:22924847|PMID:28492532|PMID:33016646 | HAMP | Human | hemochromatosis type 2B | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hemochromatosis type 2B | ClinVar | PMID:15082576|PMID:25741868|PMID:28492532 | HAMP | Human | hemochromatosis type 2B | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hemochromatosis type 2B | ClinVar | PMID:12915468|PMID:21088809|PMID:25741868|PMID:28492532 | HAMP | Human | hereditary spastic paraplegia 75 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hereditary spastic paraplegia 75 | ClinVar | PMID:28492532 | |