| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Paraparesis | HMOX1 | phenotype | C0221166 | Therapeutic | 0.2 | disgenet |
| Paraparesis | ATP13A2 | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | GJA1 | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | HMBS | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | ABCD1 | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | FUS | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | CHCHD10 | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | SLC19A3 | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | PRPS1 | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | SQSTM1 | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | SP110 | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | C9orf72 | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | HERC2 | phenotype | C0221166 | CausalMutation | 0.1 | disgenet |
| Paraparesis | TNFRSF11A | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | GJB1 | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | CYP27A1 | phenotype | C0221166 | CausalMutation | 0.1 | disgenet |
| Paraparesis | CLTC | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | NF1 | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | TARDBP | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | VCP | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | TBK1 | phenotype | C0221166 | Biomarker | 0.1 | disgenet |
| Paraparesis | SPAST | phenotype | C0221166 | GeneticVariation | 0.03 | disgenet |
| Paraparesis | ATF7IP | phenotype | C0221166 | Biomarker | 0.01 | disgenet |
| Paraparesis | CD6 | phenotype | C0221166 | Biomarker | 0.01 | disgenet |
| Paraparesis | THBS1 | phenotype | C0221166 | Biomarker | 0.01 | disgenet |
| Paraparesis | MPZ | phenotype | C0221166 | AlteredExpression | 0.01 | disgenet |
| Paraparesis | MTX1 | phenotype | C0221166 | Biomarker | 0.01 | disgenet |
| Paraparesis | CNTN3 | phenotype | C0221166 | Biomarker | 0.01 | disgenet |
| Paraparesis | MTHFR | phenotype | C0221166 | GeneticVariation | 0.01 | disgenet |
| Paraparesis | HSPD1 | phenotype | C0221166 | GeneticVariation | 0.01 | disgenet |
| Paraparesis | TRNE | phenotype | C0221166 | GeneticVariation | 0.01 | disgenet |
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