Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | IGF1 | Bonobo | Boucher-Neuhauser syndrome | | ISO | IGF1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Chorioretinal dystrophy and spinocerebellar ataxia and hypogonadotropic hypogonadism | ClinVar | | IGF1 | Bonobo | genetic disease | | ISO | IGF1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | IGF1 | Bonobo | glycogen storage disease III | | ISO | IGF1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Glycogen debrancher deficiency | ClinVar | PMID:12955720 and PMID:20301788 | IGF1 | Bonobo | Insulin-Like Growth Factor I Deficiency | | ISO | IGF1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:14684690 more ... | IGF1 | Bonobo | intellectual disability | | ISO | IGF1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Intellectual disability | ClinVar | PMID:25741868 | IGF1 | Bonobo | long QT syndrome | | ISO | IGF1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Long QT syndrome | ClinVar | PMID:26132555 | IGF1 | Bonobo | microcephaly | | ISO | IGF1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Microcephaly | ClinVar | PMID:25741868 | |