Imported Disease Annotations - CTDTerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | autosomal dominant nonsyndromic deafness 41 | | ISO | P2RX2 (Homo sapiens) | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | | epilepsy | | ISO | P2RX2 (Homo sapiens) | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:12941474 | Hyperalgesia | | ISO | P2RX2 (Homo sapiens) | 11554173 | CTD Direct Evidence: marker/mechanism | CTD | PMID:19383439 | |