Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | genetic disease | | ISO | IGF1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | Insulin-Like Growth Factor I Deficiency | | ISO | IGF1 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:15769976 more ... | intellectual disability | | ISO | IGF1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Intellectual disability | ClinVar | PMID:25741868 | microcephaly | | ISO | IGF1 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Microcephaly | ClinVar | PMID:25741868 | |