Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Chromosome 3, Monosomy 3p25 | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:21082655 | intellectual disability | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:21082655 | Neurodevelopmental Disorders | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:28191889 | |