* We recommend a score >= 0.08 for meaningful Gene-Disease associations
| GeneID | Gene_Symbol | DisGeNet_diseaseID | Disease_name | DisGeNet_sourceDB | |
| 669 | BPGM | C1291620 | Deficiency of bisphosphoglycerate mutase | 0.6 | CTD_human;ORPHANET;UNIPROT |
| 669 | BPGM | C0008325 | Cholecystitis | 0.2 | HPO |
| 669 | BPGM | C0008350 | Cholelithiasis | 0.2 | HPO |
| 669 | BPGM | C0022346 | Icterus | 0.2 | HPO |
| 669 | BPGM | C0038002 | Splenomegaly | 0.2 | HPO |
| 669 | BPGM | C0085577 | Normocytic anemia | 0.2 | HPO |
| 669 | BPGM | C0235983 | Normochromic anemia | 0.2 | HPO |
| 669 | BPGM | C4020899 | Autosomal recessive predisposition | 0.2 | HPO |
| 669 | BPGM | C4021768 | Abnormality of metabolism/homeostasis | 0.2 | HPO |
| 669 | BPGM | C4025735 | Nonspherocytic hemolytic anemia | 0.2 | HPO |