Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Msx2 | Rat | craniosynostosis 2 | | ISO | MSX2 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10742103 more ... | Msx2 | Rat | Craniosynostosis Syndrome, Autosomal Recessive | | ISO | MSX2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Craniosynostosis syndrome | ClinVar | | Msx2 | Rat | genetic disease | | ISO | MSX2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:28492532 | Msx2 | Rat | parietal foramina | | ISO | MSX2 (Homo sapiens) | 8554872 | ClinVar more ... | ClinVar | PMID:10742103 more ... | Msx2 | Rat | Parietal Foramina 1 | | ISO | MSX2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Parietal foramina 1 | ClinVar | PMID:10742103 more ... | Msx2 | Rat | Parietal Foramina with Cleidocranial Dysplasia | | ISO | MSX2 (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Parietal foramina with cleidocranial dysplasia | ClinVar | PMID:14571277 | |