Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Wnt5a | Squirrel | autosomal dominant Robinow syndrome 1 | | ISO | WNT5A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Autosomal dominant Robinow syndrome 1 | ClinVar | PMID:16602827 more ... | Wnt5a | Squirrel | Dwarfism | | ISO | WNT5A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Short stature | ClinVar | PMID:25741868 | Wnt5a | Squirrel | genetic disease | | ISO | WNT5A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 more ... | Wnt5a | Squirrel | Robinow syndrome | | ISO | WNT5A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Acral dysostosis with facial and genital abnormalities | ClinVar | PMID:18414213 more ... | |