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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