Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Hexosephosphates [NCBI]

Gene


 Gene Link Information
Gain		 01
MPO [NCBI] 6.5164e-06
NAGPA [NCBI] 4.50011e-06
HK1 [NCBI] 4.30452e-06
G6PD [NCBI] 2.59359e-06
CTSL1 [NCBI] 2.54565e-06
FPGT [NCBI] 2.464e-06
LGTN [NCBI] 2.34953e-06
ALDOC [NCBI] 2.26963e-06
H6PD [NCBI] 2.15827e-06
PRPS1 [NCBI] 2.15827e-06
MPI [NCBI] 2.07988e-06
PGD [NCBI] 2.07988e-06
M6PR [NCBI] 2.03323e-06
GCKR [NCBI] 1.97569e-06
HEXB [NCBI] 1.86437e-06
GALT [NCBI] 1.81592e-06
REN [NCBI] 1.67995e-06
MAN1C1 [NCBI] 1.65629e-06
GCK [NCBI] 1.64941e-06
TF [NCBI] 1.14771e-06
ACP5 [NCBI] 1.12999e-06
TG [NCBI] 1.05924e-06
EGF [NCBI] 5.19074e-07



OMIM


 OMIM Link Information
gain		 01
mannose 6-phosphate receptor recognition defect, lebanese type [NCBI] 0.00277021
galactosemia [NCBI] 0.000431387
mucolipidosis ii [NCBI] 0.00031018
CGD [NCBI] 0.000171615
IGF2R [NCBI] 0.000129792
PHA [NCBI] 0.000111755
myeloperoxidase deficiency [NCBI] 0.000106042
glycogen storage disease ib [NCBI] 9.16146e-05
GPX1 [NCBI] 9.01516e-05
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i [NCBI] 8.99052e-05
LAD [NCBI] 7.90344e-05
pyruvate kinase deficiency of red cells [NCBI] 7.70959e-05
GPI [NCBI] 7.62574e-05
G6PD [NCBI] 6.70306e-05
WBS [NCBI] 6.28782e-05
GALT [NCBI] 5.04972e-05
FPGT [NCBI] 4.81542e-05
MPO [NCBI] 4.60794e-05
PKM2 [NCBI] 2.92835e-05
MPI [NCBI] 2.77988e-05
ALDOA [NCBI] 2.74843e-05
HK1 [NCBI] 2.54731e-05
fructose intolerance, hereditary [NCBI] 2.26247e-05
GSR [NCBI] 2.17259e-05
CTSL [NCBI] 2.1328e-05
ITGB2 [NCBI] 2.1328e-05
IGF2 [NCBI] 2.07822e-05
H6PD [NCBI] 1.87325e-05
SLE [NCBI] 1.1331e-05
TF [NCBI] 6.7852e-06
TG [NCBI] 4.93208e-06
EGF [NCBI] 3.81021e-07



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