| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Peroxisome Biogenesis Disorder, Complementation Group H | HTC2 | disease | C1866260 | GeneticVariation | 0.06 | disgenet |
| Peroxisome Biogenesis Disorder, Complementation Group H | HTC2 | disease | C1866260 | Biomarker | 0.06 | disgenet |
| Peroxisome Biogenesis Disorder, Complementation Group H | HTC2 | disease | C1866260 | AlteredExpression | 0.06 | disgenet |
| Peroxisome Biogenesis Disorder, Complementation Group H | CCND1 | disease | C1866260 | GeneticVariation | 0.01 | disgenet |
| Peroxisome Biogenesis Disorder, Complementation Group H | ERBB2 | disease | C1866260 | Biomarker | 0.01 | disgenet |
| Peroxisome Biogenesis Disorder, Complementation Group H | AKT2 | disease | C1866260 | Biomarker | 0.01 | disgenet |
| Peroxisome Biogenesis Disorder, Complementation Group H | BRCA1 | disease | C1866260 | Biomarker | 0.01 | disgenet |
| Peroxisome Biogenesis Disorder, Complementation Group H | FGFR1 | disease | C1866260 | AlteredExpression | 0.01 | disgenet |
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