* We recommend a score >= 0.08 for meaningful Gene-Disease associations
GeneID | Gene_Symbol | DisGeNet_diseaseID | Disease_name | ![]() | DisGeNet_sourceDB |
5537 | PPP6C | C0025202 | melanoma | 0.201098907136852 | BEFREE;CTD_human |
5537 | PPP6C | C0007117 | Basal cell carcinoma | 0.2 | CTD_human |
5537 | PPP6C | C0007115 | Malignant neoplasm of thyroid | 0.0002747267842131 | BEFREE |
5537 | PPP6C | C0033860 | Psoriasis | 0.0002747267842131 | BEFREE |
5537 | PPP6C | C0278883 | Metastatic melanoma | 0.0002747267842131 | BEFREE |
5537 | PPP6C | C0332996 | Persistent embryonic structure | 0.0002747267842131 | BEFREE |
5537 | PPP6C | C0345967 | Malignant mesothelioma | 0.0002747267842131 | BEFREE |
5537 | PPP6C | C0549473 | Thyroid carcinoma | 0.0002747267842131 | BEFREE |
5537 | PPP6C | C1290375 | Mesothelioma (malignant, clinical disorder) (disorder) | 0.0002747267842131 | BEFREE |
5537 | PPP6C | C1621958 | Glioblastoma Multiforme | 0.0002747267842131 | BEFREE |
5537 | PPP6C | C2239176 | Liver carcinoma | 0.0002747267842131 | BEFREE |