| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Congenital disorder of glycosylation type II | ALG2 | disease | C1842836 | CausalMutation | 0.6 | disgenet |
| Congenital disorder of glycosylation type II | ALG2 | disease | C1842836 | Biomarker | 0.6 | disgenet |
| Congenital disorder of glycosylation type II | MAN1B1 | disease | C1842836 | Biomarker | 0.02 | disgenet |
| Congenital disorder of glycosylation type II | SLC39A8 | disease | C1842836 | GeneticVariation | 0.01 | disgenet |
| Congenital disorder of glycosylation type II | COG1 | disease | C1842836 | Biomarker | 0.01 | disgenet |
| Congenital disorder of glycosylation type II | COG8 | disease | C1842836 | Biomarker | 0.01 | disgenet |
| Congenital disorder of glycosylation type II | COG4 | disease | C1842836 | GeneticVariation | 0.01 | disgenet |
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