Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | autistic disorder | | ISO | FOXO4 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Autism | ClinVar | PMID:21681106 and PMID:30208311 | FG Syndrome 1 | | ISO | FOXO4 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: FG syndrome 1 | ClinVar | PMID:28492532 | genetic disease | | ISO | FOXO4 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | | intellectual disability | | ISO | FOXO4 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Intellectual disability | ClinVar | | Macrocephaly | | ISO | FOXO4 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Macrocephaly | ClinVar | PMID:25741868 | syndromic X-linked intellectual disability Lubs type | | ISO | FOXO4 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Syndromic X-linked intellectual disability Lubs type | ClinVar | PMID:25741868 | |