Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Mt-nd3 | Rat | cerebellar ataxia | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cerebellar ataxia | ClinVar | PMID:10590437 more ... | Mt-nd3 | Rat | cone-rod dystrophy | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Rod-cone dystrophy | ClinVar | PMID:10590437 more ... | Mt-nd3 | Rat | dilated cardiomyopathy | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Primary dilated cardiomyopathy | ClinVar | PMID:24088041 and PMID:26633545 | Mt-nd3 | Rat | Hypertelorism | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hypertelorism | ClinVar | PMID:10590437 more ... | Mt-nd3 | Rat | Kearns-Sayre syndrome | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Kearns-Sayre syndrome | ClinVar | PMID:20301382 | Mt-nd3 | Rat | Leber congenital amaurosis | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Leber's disease | ClinVar | PMID:10590437 more ... | Mt-nd3 | Rat | Leber hereditary optic neuropathy | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10590437 more ... | Mt-nd3 | Rat | Leber hereditary optic neuropathy and dystonia | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Dystonia familial and with visual failure and striatal lucencies | ClinVar | PMID:17152068 more ... | Mt-nd3 | Rat | Leigh disease | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10590437 more ... | Mt-nd3 | Rat | mitochondrial complex I deficiency | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Mitochondrial complex I deficiency | ClinVar | PMID:11456298 more ... | Mt-nd3 | Rat | mitochondrial complex V (ATP synthase) deficiency mitochondrial type 1 | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Mitochondrial complex v (atp synthase) deficiency and mitochondrial type 1 | ClinVar | PMID:10590437 more ... | Mt-nd3 | Rat | mitochondrial metabolism disease | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Mitochondrial disease | ClinVar | PMID:10590437 more ... | Mt-nd3 | Rat | mitochondrial type mitochondrial complex I deficiency 1 | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: MITOCHONDRIAL COMPLEX I DEFICIENCY and MITOCHONDRIAL TYPE 1 | ClinVar | PMID:11456298 more ... | Mt-nd3 | Rat | Multiple mitochondrial dysfunctions syndrome 8 | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Mitochondrial myopathy more ... | ClinVar | PMID:17152068 more ... | Mt-nd3 | Rat | NARP syndrome | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: NARP syndrome | ClinVar | PMID:10590437 more ... | Mt-nd3 | Rat | Parkinson's disease | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Parkinson disease and resistance to | ClinVar | PMID:17066297 more ... | Mt-nd3 | Rat | Pearson syndrome | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Pearson syndrome | ClinVar | | Mt-nd3 | Rat | Premature Birth | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Premature birth | ClinVar | PMID:10590437 more ... | Mt-nd3 | Rat | Subacute Necrotizing Encephalopathy of Leigh, Infantile | | ISO | MT-ND3 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Leigh's necrotizing encephalopathy | ClinVar | PMID:10590437 more ... | |