Gendoo

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01 Glycogen Storage Disease Type I [NCBI]

Gene


 Gene Link Information
Gain		 01
SLC37A4 [NCBI] 0.000906176
G6PC [NCBI] 0.000416242
G6PD [NCBI] 8.38151e-05
PHKA2 [NCBI] 2.04421e-05
SLC17A3 [NCBI] 1.19907e-05
FXYD2 [NCBI] 9.88006e-06
AK1 [NCBI] 9.36125e-06
G6PC2 [NCBI] 9.36125e-06
HAX1 [NCBI] 8.28877e-06
CXCL2 [NCBI] 7.93084e-06
HAMP [NCBI] 6.60786e-06
HSD11B1 [NCBI] 6.14441e-06
GAA [NCBI] 5.65913e-06
ACVRL1 [NCBI] 5.46826e-06
SCARB1 [NCBI] 5.35218e-06
BMPR2 [NCBI] 4.97748e-06
UGT1A1 [NCBI] 3.72969e-06
HNF1B [NCBI] 3.54966e-06
HNF1A [NCBI] 3.40919e-06
UMOD [NCBI] 3.16175e-06
IL8 [NCBI] 2.93377e-06
PTK2 [NCBI] 2.82455e-06
LPL [NCBI] 1.54705e-06
BAX [NCBI] 8.96773e-07
VWF [NCBI] 8.5703e-07
AFP [NCBI] 7.57293e-07
PCNA [NCBI] 6.20836e-07
APOE [NCBI] 5.75545e-07



OMIM


 OMIM Link Information
gain		 01
glycogen storage disease i [NCBI] 0.00395956
glycogen storage disease ib [NCBI] 0.00359891
G6PT1 [NCBI] 0.00111789
glycogen storage disease ic [NCBI] 0.000932362
G6PD [NCBI] 0.000272676
glycogen storage disease iii [NCBI] 0.000210954
glycogen storage disease ixa [NCBI] 0.000119372
glycogen storage disease 0, liver [NCBI] 7.86521e-05
acyl-coa dehydrogenase, long-chain, deficiency of [NCBI] 7.86521e-05
SLC17A3 [NCBI] 5.91585e-05
FXYD2 [NCBI] 5.91585e-05
G6PC3 [NCBI] 5.91585e-05
mucopolysaccharidosis type iiib [NCBI] 5.86222e-05
refsum disease, infantile form [NCBI] 5.59978e-05
AGL [NCBI] 3.72056e-05
AK1 [NCBI] 3.26297e-05
CSF3 [NCBI] 2.49167e-05
HNF1A [NCBI] 2.27548e-05
tyrosinemia, type i [NCBI] 2.16943e-05
CEACAM5 [NCBI] 6.90367e-06
PTK2 [NCBI] 4.93991e-06
PCNA [NCBI] 1.82088e-06
AFP [NCBI] 1.04666e-06
APOE [NCBI] 3.28846e-07
LPL [NCBI] 2.75776e-07



Database Center for Life Science