Disease Information |
Disease Name |
Gene Name |
Type |
UMLS |
Association Type |
Score |
Source |
Peroxisome Biogenesis Disorder, Complementation Group G |
FRAXA |
disease |
C1864172 |
GeneticVariation |
0.01 |
disgenet |
Peroxisome Biogenesis Disorder, Complementation Group G |
GLS |
disease |
C1864172 |
GeneticVariation |
0.01 |
disgenet |
Peroxisome Biogenesis Disorder, Complementation Group G |
SLC22A5 |
disease |
C1864172 |
GeneticVariation |
0.01 |
disgenet |
Peroxisome Biogenesis Disorder, Complementation Group G |
GGCT |
disease |
C1864172 |
GeneticVariation |
0.01 |
disgenet |
Peroxisome Biogenesis Disorder, Complementation Group G |
TYR |
disease |
C1864172 |
GeneticVariation |
0.01 |
disgenet |
Peroxisome Biogenesis Disorder, Complementation Group G |
FRAXE |
disease |
C1864172 |
GeneticVariation |
0.01 |
disgenet |
Peroxisome Biogenesis Disorder, Complementation Group G |
FMR1 |
disease |
C1864172 |
GeneticVariation |
0.01 |
disgenet |
Peroxisome Biogenesis Disorder, Complementation Group G |
LDLR |
disease |
C1864172 |
GeneticVariation |
0.01 |
disgenet |
Peroxisome Biogenesis Disorder, Complementation Group G |
DOCK11 |
disease |
C1864172 |
GeneticVariation |
0.01 |
disgenet |
Peroxisome Biogenesis Disorder, Complementation Group G |
AGA |
disease |
C1864172 |
GeneticVariation |
0.01 |
disgenet |
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