Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | Boucher-Neuhauser syndrome | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | | hereditary spastic paraplegia | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:20382209 | hereditary spastic paraplegia 39 | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | | Laurence-Moon syndrome | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | | motor neuron disease | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:18313024 and PMID:20603202 | nervous system disease | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:8211998 | Oliver-McFarlane syndrome | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | | peripheral nervous system disease | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:20188121 | polyneuropathy | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:22819951 | sick building syndrome | | EXP | | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:23418070 | |