Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Spastic paraplegia 10, autosomal dominant KIF5A disease C1858712 Biomarker 0.76 orphanet , disgenet
Spastic paraplegia 10, autosomal dominant KIF5A disease C1858712 GermlineCausalMutation 0.76 orphanet , disgenet
Spastic paraplegia 10, autosomal dominant KIF5A disease C1858712 CausalMutation 0.76 orphanet , disgenet
Spastic paraplegia 10, autosomal dominant KIF5A disease C1858712 GeneticVariation 0.76 orphanet , disgenet
Spastic paraplegia 10, autosomal dominant SPAST disease C1858712 GeneticVariation 0.08 disgenet
Spastic paraplegia 10, autosomal dominant SPAST disease C1858712 Biomarker 0.08 disgenet
Spastic paraplegia 10, autosomal dominant ATL1 disease C1858712 Biomarker 0.03 disgenet
Spastic paraplegia 10, autosomal dominant ATL1 disease C1858712 GeneticVariation 0.03 disgenet
Spastic paraplegia 10, autosomal dominant KIF1B disease C1858712 Biomarker 0.02 disgenet
Spastic paraplegia 10, autosomal dominant MAD2L1BP disease C1858712 Biomarker 0.02 disgenet
Spastic paraplegia 10, autosomal dominant IFIH1 disease C1858712 Biomarker 0.01 disgenet
Spastic paraplegia 10, autosomal dominant CPT1C disease C1858712 GeneticVariation 0.01 orphanet , disgenet
Spastic paraplegia 10, autosomal dominant REEP1 disease C1858712 Biomarker 0.01 disgenet
Spastic paraplegia 10, autosomal dominant S100A4 disease C1858712 Biomarker 0.01 disgenet
Spastic paraplegia 10, autosomal dominant SNTB1 disease C1858712 Biomarker 0.01 disgenet
Spastic paraplegia 10, autosomal dominant KIF5C disease C1858712 GeneticVariation 0.01 disgenet
Spastic paraplegia 10, autosomal dominant DNM2 disease C1858712 GeneticVariation 0.01 disgenet
Spastic paraplegia 10, autosomal dominant KIF1A disease C1858712 GeneticVariation 0.01 disgenet
Spastic paraplegia 10, autosomal dominant SLC33A1 disease C1858712 GeneticVariation 0.01 disgenet
Spastic paraplegia 10, autosomal dominant KIF5B disease C1858712 GeneticVariation 0.01 disgenet
Spastic paraplegia 10, autosomal dominant UBAP1 disease C1858712 GeneticVariation 0.01 disgenet
Spastic paraplegia 10, autosomal dominant SPG41 NA C1858712 NA NA orphanet
Spastic paraplegia 10, autosomal dominant FAR1 NA C1858712 NA NA orphanet
Spastic paraplegia 10, autosomal dominant ALDH18A1 NA C1858712 NA NA orphanet
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