| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Prieto X-linked mental retardation syndrome | SOX9 | disease | C1839730 | AlteredExpression | 0.08 | disgenet |
| Prieto X-linked mental retardation syndrome | SOX9 | disease | C1839730 | GeneticVariation | 0.08 | disgenet |
| Prieto X-linked mental retardation syndrome | SOX9 | disease | C1839730 | Biomarker | 0.08 | disgenet |
| Prieto X-linked mental retardation syndrome | PAX2 | disease | C1839730 | GeneticVariation | 0.04 | disgenet |
| Prieto X-linked mental retardation syndrome | DLX6 | disease | C1839730 | GeneticVariation | 0.01 | disgenet |
| Prieto X-linked mental retardation syndrome | BMPR1B | disease | C1839730 | Biomarker | 0.01 | disgenet |
| Prieto X-linked mental retardation syndrome | GRM4 | disease | C1839730 | GeneticVariation | 0.01 | disgenet |
| Prieto X-linked mental retardation syndrome | MED13L | disease | C1839730 | Biomarker | 0.01 | disgenet |
| Prieto X-linked mental retardation syndrome | KCNJ2 | disease | C1839730 | AlteredExpression | 0.01 | disgenet |
| Prieto X-linked mental retardation syndrome | PHAX | disease | C1839730 | Biomarker | 0.01 | disgenet |
| Prieto X-linked mental retardation syndrome | FBN2 | disease | C1839730 | Biomarker | 0.01 | disgenet |
| Prieto X-linked mental retardation syndrome | IRF6 | disease | C1839730 | GeneticVariation | 0.01 | disgenet |
| Prieto X-linked mental retardation syndrome | KCNJ16 | disease | C1839730 | Biomarker | 0.01 | disgenet |
| Prieto X-linked mental retardation syndrome | DLX5 | disease | C1839730 | GeneticVariation | 0.01 | disgenet |
| Prieto X-linked mental retardation syndrome | BMP2 | disease | C1839730 | Biomarker | 0.01 | disgenet |
| Prieto X-linked mental retardation syndrome | KIF15 | disease | C1839730 | GeneticVariation | 0.01 | disgenet |
| Prieto X-linked mental retardation syndrome | PRS | disease | C1839730 | Biomarker | 0.01 | disgenet |
| Prieto X-linked mental retardation syndrome | WNT1 | disease | C1839730 | GeneticVariation | 0.01 | disgenet |
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