| Disease Information | ||||||
|---|---|---|---|---|---|---|
| Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
| Spastic paraplegia 12, autosomal dominant | RTN2 | disease | C1858106 | GeneticVariation | 0.7 | orphanet , disgenet |
| Spastic paraplegia 12, autosomal dominant | RTN2 | disease | C1858106 | CausalMutation | 0.7 | orphanet , disgenet |
| Spastic paraplegia 12, autosomal dominant | RTN2 | disease | C1858106 | GermlineCausalMutation | 0.7 | orphanet , disgenet |
| Spastic paraplegia 12, autosomal dominant | RTN2 | disease | C1858106 | Biomarker | 0.7 | orphanet , disgenet |
| Spastic paraplegia 12, autosomal dominant | PPM1N | disease | C1858106 | CausalMutation | 0.1 | disgenet |
| Spastic paraplegia 12, autosomal dominant | PPM1N | disease | C1858106 | GeneticVariation | 0.1 | disgenet |
| Spastic paraplegia 12, autosomal dominant | UBAP1 | NA | C1858106 | NA | NA | orphanet |
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