Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | FGF8 | Bonobo | genetic disease | | ISO | FGF8 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | FGF8 | Bonobo | holoprosencephaly | | ISO | FGF8 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:20463092 more ... | FGF8 | Bonobo | holoprosencephaly 1 | | ISO | FGF8 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Holoprosencephaly 1 | ClinVar | PMID:18596921 more ... | FGF8 | Bonobo | hypogonadotropic hypogonadism 6 with or without anosmia | | ISO | FGF8 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hypogonadotropic hypogonadism 6 with or without anosmia | ClinVar | PMID:17360555 more ... | FGF8 | Bonobo | HYPOPLASTIC FEMURS AND PELVIS | | ISO | FGF8 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Hypoplastic femurs and pelvis | ClinVar | PMID:34433009 | FGF8 | Bonobo | Kallmann Syndrome 6 | | ISO | FGF8 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Kallmann syndrome 6 | ClinVar | PMID:22399515 more ... | FGF8 | Bonobo | microcephaly | | ISO | FGF8 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Microcephaly | ClinVar | PMID:25741868 | FGF8 | Bonobo | Peters plus syndrome | | ISO | FGF8 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Peters plus syndrome | ClinVar | PMID:25741868 more ... | FGF8 | Bonobo | spermatogenic failure 57 | | ISO | FGF8 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Male infertility with azoospermia or oligozoospermia due to single gene mutation | ClinVar | PMID:25741868 | |