| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Myoglobinuria, Recurrent | COX1 | phenotype | C1838877 | CausalMutation | 0.1 | disgenet |
| Myoglobinuria, Recurrent | COQ2 | phenotype | C1838877 | Biomarker | 0.1 | disgenet |
| Myoglobinuria, Recurrent | MT-CO3 | NA | C1838877 | NA | NA | orphanet |
| Myoglobinuria, Recurrent | LPIN1 | NA | C1838877 | NA | NA | orphanet |
| Myoglobinuria, Recurrent | MT-CO1 | NA | C1838877 | NA | NA | orphanet |
| click here to return to the previous page | ||||||