Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Dbh | Mouse | developmental and epileptic encephalopathy 14 | | ISO | DBH (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Developmental and epileptic encephalopathy and 14 | ClinVar | PMID:28492532 | Dbh | Mouse | dopamine beta-hydroxylase deficiency | | ISO | DBH (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Orthostatic hypotension 1 | ClinVar | PMID:11170900 more ... | Dbh | Mouse | Ehlers-Danlos syndrome classic type 1 | | ISO | DBH (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Ehlers-Danlos syndrome and classic type | ClinVar | PMID:28492532 | Dbh | Mouse | genetic disease | | ISO | DBH (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:17576681 more ... | Dbh | Mouse | Kleefstra syndrome 1 | | ISO | DBH (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Kleefstra syndrome 1 | ClinVar | PMID:22318994 more ... | Dbh | Mouse | Leigh disease | | ISO | DBH (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Leigh syndrome | ClinVar | PMID:28492532 | Dbh | Mouse | primary coenzyme Q10 deficiency 7 | | ISO | DBH (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome | ClinVar | PMID:28492532 | Dbh | Mouse | Rafiq syndrome | | ISO | DBH (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Rafiq syndrome | ClinVar | PMID:28492532 | Dbh | Mouse | sensorineural hearing loss | | ISO | DBH (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Sensorineural hearing loss disorder | ClinVar | PMID:25741868 | Dbh | Mouse | tuberous sclerosis 1 | | ISO | DBH (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Tuberous sclerosis 1 | ClinVar | PMID:28492532 | |