Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Mt-co3 | Rat | cerebellar ataxia | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cerebellar ataxia | ClinVar | PMID:10590437 more ... | Mt-co3 | Rat | cone-rod dystrophy | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Rod-cone dystrophy | ClinVar | PMID:10590437 more ... | Mt-co3 | Rat | cytochrome-c oxidase deficiency disease | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: COX deficiency | ClinVar | PMID:12414820 more ... | Mt-co3 | Rat | dilated cardiomyopathy | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Primary dilated cardiomyopathy | ClinVar | PMID:24088041 and PMID:26633545 | Mt-co3 | Rat | epilepsy | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Epilepsy | ClinVar | PMID:28027978 | Mt-co3 | Rat | Hypertelorism | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hypertelorism | ClinVar | PMID:10590437 more ... | Mt-co3 | Rat | Kearns-Sayre syndrome | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Kearns-Sayre syndrome | ClinVar | PMID:20301382 | Mt-co3 | Rat | lactic acidosis | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Seizures and lactic acidosis | ClinVar | PMID:12915481 and PMID:8739943 | Mt-co3 | Rat | Leber congenital amaurosis | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Leber's disease | ClinVar | PMID:10590437 more ... | Mt-co3 | Rat | Leber hereditary optic neuropathy | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10590437 more ... | Mt-co3 | Rat | Leigh disease | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10590437 more ... | Mt-co3 | Rat | MELAS syndrome | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Juvenile myopathy more ... | ClinVar | PMID:15823923 more ... | Mt-co3 | Rat | mitochondrial complex IV deficiency nuclear type 1 | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Mitochondrial complex IV deficiency and nuclear type 1 | ClinVar | PMID:11063732 more ... | Mt-co3 | Rat | mitochondrial complex V (ATP synthase) deficiency mitochondrial type 1 | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Mitochondrial complex v (atp synthase) deficiency and mitochondrial type 1 | ClinVar | PMID:10590437 more ... | Mt-co3 | Rat | mitochondrial metabolism disease | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10590437 more ... | Mt-co3 | Rat | Mitochondrial Myopathy, Infantile, Transient | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Mitochondrial myopathy more ... | ClinVar | PMID:12414820 | Mt-co3 | Rat | NARP syndrome | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: NARP syndrome | ClinVar | PMID:10590437 more ... | Mt-co3 | Rat | nephrolithiasis | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Nephrolithiasis | ClinVar | PMID:25741868 | Mt-co3 | Rat | Pearson syndrome | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pearson syndrome | ClinVar | | Mt-co3 | Rat | Premature Birth | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Premature birth | ClinVar | PMID:10590437 more ... | Mt-co3 | Rat | Subacute Necrotizing Encephalopathy of Leigh, Infantile | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Leigh's necrotizing encephalopathy | ClinVar | PMID:10590437 more ... | Mt-co3 | Rat | tetralogy of Fallot | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Tetralogy of Fallot | ClinVar | | Mt-co3 | Rat | Venous Thromboembolism | | ISO | MT-CO3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Venous thromboembolism | ClinVar | | |