Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Fabry Disease	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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