| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Peroxisome Biogenesis Disorder, Complementation Group C | CA2 | disease | C1832232 | GeneticVariation | 0.03 | disgenet |
| Peroxisome Biogenesis Disorder, Complementation Group C | TGM2 | disease | C1832232 | GeneticVariation | 0.03 | disgenet |
| Peroxisome Biogenesis Disorder, Complementation Group C | SLC25A20 | disease | C1832232 | GeneticVariation | 0.03 | disgenet |
| Peroxisome Biogenesis Disorder, Complementation Group C | CYP17A1 | disease | C1832232 | GeneticVariation | 0.02 | disgenet |
| Peroxisome Biogenesis Disorder, Complementation Group C | GGCT | disease | C1832232 | GeneticVariation | 0.01 | disgenet |
| Peroxisome Biogenesis Disorder, Complementation Group C | SLC22A1 | disease | C1832232 | Biomarker | 0.01 | disgenet |
| Peroxisome Biogenesis Disorder, Complementation Group C | ERBB2 | disease | C1832232 | Biomarker | 0.01 | disgenet |
| Peroxisome Biogenesis Disorder, Complementation Group C | DNLZ | disease | C1832232 | Biomarker | 0.01 | disgenet |
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