Imported Disease Annotations - ClinVarObject Symbol | Species | Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | OPRM1 | Human | autosomal recessive spinocerebellar ataxia 8 | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Autosomal recessive ataxia and Beauce type | ClinVar | PMID:19542096 more ... | OPRM1 | Human | chromosome 6q24-q25 deletion syndrome | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Chromosome 6q24-q25 deletion syndrome | ClinVar | PMID:25741868 and PMID:38177409 | OPRM1 | Human | opiate dependence | | IAGP | (Homo sapiens) | 8554872 | ClinVar Annotator: match by term: Opioid dependence more ... | ClinVar | PMID:11134674 more ... | |