Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Mt-nd1 | Rat | Alzheimer's disease | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Alzheimer disease | ClinVar | PMID:15972314 and PMID:8104867 | Mt-nd1 | Rat | aminoglycoside-induced deafness | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: STREPTOMYCIN OTOTOXICITY | ClinVar | PMID:10521300 more ... | Mt-nd1 | Rat | autosomal-mitochondrial sensorineural deafness | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Deafness more ... | ClinVar | PMID:10521300 more ... | Mt-nd1 | Rat | cerebellar ataxia | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Cerebellar ataxia | ClinVar | PMID:10590437 more ... | Mt-nd1 | Rat | colon carcinoma | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Carcinoma of colon | ClinVar | PMID:10519336 more ... | Mt-nd1 | Rat | cone-rod dystrophy | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Rod-cone dystrophy | ClinVar | PMID:10590437 more ... | Mt-nd1 | Rat | Developmental Disabilities | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Global developmental delay | ClinVar | PMID:25741868 and PMID:28027978 | Mt-nd1 | Rat | dystonia | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Dystonia and adult-onset | ClinVar | PMID:11938495 more ... | Mt-nd1 | Rat | Hypertelorism | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hypertelorism | ClinVar | PMID:10590437 more ... | Mt-nd1 | Rat | late onset Parkinson's disease | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Parkinson disease and late-onset | ClinVar | PMID:15972314 and PMID:8104867 | Mt-nd1 | Rat | Leber congenital amaurosis | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Leber's disease | ClinVar | PMID:10590437 more ... | Mt-nd1 | Rat | Leber hereditary optic neuropathy | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10590437 more ... | Mt-nd1 | Rat | Leigh disease | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10519336 more ... | Mt-nd1 | Rat | MELAS syndrome | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:15466014 more ... | Mt-nd1 | Rat | migraine | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Migraine | ClinVar | PMID:15466014 more ... | Mt-nd1 | Rat | mitochondrial complex V (ATP synthase) deficiency mitochondrial type 1 | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Mitochondrial complex v (atp synthase) deficiency and mitochondrial type 1 | ClinVar | PMID:10590437 more ... | Mt-nd1 | Rat | mitochondrial metabolism disease | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10521300 more ... | Mt-nd1 | Rat | Mitochondrial Myopathy, Infantile, Transient | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:25741868 | Mt-nd1 | Rat | mitochondrial nonsyndromic sensorineural deafness | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Deafness more ... | ClinVar | PMID:10521300 more ... | Mt-nd1 | Rat | NARP syndrome | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: NARP syndrome | ClinVar | PMID:10590437 more ... | Mt-nd1 | Rat | optic nerve disease | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Optic nerve disorder | ClinVar | PMID:20301353 and PMID:30143805 | Mt-nd1 | Rat | Premature Birth | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Premature birth | ClinVar | PMID:10590437 more ... | Mt-nd1 | Rat | ptosis | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Ptosis | ClinVar | PMID:25741868 | Mt-nd1 | Rat | restrictive cardiomyopathy | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Restrictive cardiomyopathy | ClinVar | PMID:10521300 more ... | Mt-nd1 | Rat | Subacute Necrotizing Encephalopathy of Leigh, Infantile | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Leigh's necrotizing encephalopathy | ClinVar | PMID:10590437 more ... | Mt-nd1 | Rat | sudden infant death syndrome | | ISO | MT-ND1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: SUDDEN INFANT DEATH SYNDROME | ClinVar | PMID:10519336 more ... | |