Imported Disease Annotations - ClinVarTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | autosomal dominant Robinow syndrome 1 | | ISO | WNT5A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Autosomal dominant Robinow syndrome 1 | ClinVar | PMID:16602827 more ... | genetic disease | | ISO | WNT5A (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:25741868 and PMID:28492532 | |