Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Tgfb2 | Naked Mole-Rat | aortic aneurysm | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Aortic aneurysm | ClinVar | PMID:22772371 more ... | Tgfb2 | Naked Mole-Rat | aortic disease | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Familial aortopathy | ClinVar | PMID:22772368 more ... | Tgfb2 | Naked Mole-Rat | atrial heart septal defect 1 | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Atrial septal defect 1 | ClinVar | | Tgfb2 | Naked Mole-Rat | connective tissue disease | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 and PMID:28492532 | Tgfb2 | Naked Mole-Rat | Ehlers-Danlos syndrome | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Ehlers-Danlos syndrome | ClinVar | PMID:22772371 more ... | Tgfb2 | Naked Mole-Rat | gastrointestinal stromal tumor | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Gastrointestinal stromal tumor | ClinVar | PMID:28492532 | Tgfb2 | Naked Mole-Rat | genetic disease | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | Tgfb2 | Naked Mole-Rat | Hirschsprung Disease 1 | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hirschsprung disease 1 | ClinVar | PMID:25741868 more ... | Tgfb2 | Naked Mole-Rat | Hirschsprung's disease | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hirschsprung disease more ... | ClinVar | PMID:25741868 more ... | Tgfb2 | Naked Mole-Rat | Holt-Oram syndrome | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Holt-Oram syndrome | ClinVar | PMID:24465802 more ... | Tgfb2 | Naked Mole-Rat | Loeys-Dietz syndrome | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10611753 more ... | Tgfb2 | Naked Mole-Rat | Loeys-Dietz syndrome 4 | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Loeys-Dietz syndrome 4 | ClinVar | PMID:10611753 more ... | Tgfb2 | Naked Mole-Rat | lung adenocarcinoma | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Lung adenocarcinoma | ClinVar | PMID:27993330 | Tgfb2 | Naked Mole-Rat | Martsolf Syndrome | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Martsolf syndrome | ClinVar | PMID:23420520 and PMID:28492532 | Tgfb2 | Naked Mole-Rat | parathyroid carcinoma | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Parathyroid carcinoma | ClinVar | PMID:28492532 | Tgfb2 | Naked Mole-Rat | thoracic aortic aneurysm | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10611753 more ... | Tgfb2 | Naked Mole-Rat | thoracic aortic aneurysm | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10611753 more ... | Tgfb2 | Naked Mole-Rat | thoracic aortic aneurysm | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10611753 more ... | Tgfb2 | Naked Mole-Rat | thoracic aortic aneurysm | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10611753 more ... | Tgfb2 | Naked Mole-Rat | thoracic aortic aneurysm | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10611753 more ... | Tgfb2 | Naked Mole-Rat | thoracic aortic aneurysm | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Thoracic aortic aneurysms and dissections | ClinVar | PMID:10611753 more ... | Tgfb2 | Naked Mole-Rat | thoracic aortic aneurysm | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Thoracic aortic aneurysms and dissections | ClinVar | PMID:22772368 more ... | Tgfb2 | Naked Mole-Rat | Usher syndrome | | ISO | TGFB2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Usher syndrome | ClinVar | PMID:28041643 | |