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MeSH keywords -> Related genes, diseases (OMIM)


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01 Fabry Disease [NCBI]


Gene


Gene Link Information
Gain
01
GLA [NCBI] 0.000951894
KTWS [NCBI] 0.000332969
NAGA [NCBI] 0.000152511
RPL36A [NCBI] 1.18261e-05
SAR1B [NCBI] 1.07595e-05
SPTLC1 [NCBI] 8.96411e-06
PRKAA1 [NCBI] 8.34837e-06
PRKAG2 [NCBI] 8.16474e-06
RPGRIP1 [NCBI] 7.94711e-06
CST3 [NCBI] 7.505e-06
LAMP2 [NCBI] 7.27959e-06
RAB7A [NCBI] 7.08423e-06
MYBPC3 [NCBI] 6.96546e-06
NDP [NCBI] 6.67618e-06
VCAM1 [NCBI] 5.79328e-06
NAIP [NCBI] 5.77903e-06
GBA [NCBI] 5.7509e-06
NOS3 [NCBI] 5.71694e-06
PSAP [NCBI] 5.61692e-06
SELE [NCBI] 5.43419e-06
ICAM1 [NCBI] 4.23441e-06
IL1A [NCBI] 4.00713e-06
CRP [NCBI] 3.8911e-06
BTK [NCBI] 3.88663e-06
UMOD [NCBI] 3.55755e-06
MUC1 [NCBI] 3.32605e-06
IL1B [NCBI] 2.70056e-06
IL10 [NCBI] 2.38418e-06
VDR [NCBI] 2.30463e-06
ACE [NCBI] 2.1962e-06
IL6 [NCBI] 1.89953e-06
NOS2 [NCBI] 1.60592e-06
MPO [NCBI] 1.0794e-06
TNF [NCBI] 8.93482e-09




OMIM


OMIM Link Information
gain
01
fabry disease [NCBI] 0.0110998
GLA [NCBI] 0.00293526
CTPP1 [NCBI] 0.00116675
kanzaki disease [NCBI] 0.000754286
NAGA [NCBI] 0.000188004
SLE [NCBI] 0.000185947
angiokeratoma corporis diffusum with arteriovenous fistulas [NCBI] 0.000107338
aspartylglucosaminuria [NCBI] 8.65527e-05
fucosidosis [NCBI] 8.59037e-05
CMTC [NCBI] 8.23885e-05
mucolipidosis iii, complementation group c [NCBI] 5.86268e-05
LAMP2 [NCBI] 4.76952e-05
mannosidosis, beta a, lysosomal [NCBI] 4.70218e-05
danon disease [NCBI] 4.33852e-05
gm1-gangliosidosis, type iii [NCBI] 4.25959e-05
gm1-gangliosidosis, type i [NCBI] 3.5383e-05
GLB1 [NCBI] 3.52388e-05
neuraminidase deficiency with beta-galactosidase deficiency [NCBI] 3.29016e-05
NOS3 [NCBI] 3.1408e-05
mucolipidosis ii [NCBI] 2.72025e-05
BTK [NCBI] 2.50203e-05
metachromatic leukodystrophy [NCBI] 2.26441e-05
TSD [NCBI] 9.99165e-06
CHS [NCBI] 9.50402e-06




Database Center for Life Science