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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hypoxanthines [NCBI]


Gene


Gene Link Information
Gain
01
ADA [NCBI] 1.21255e-05
APRT [NCBI] 1.11512e-05
CAT [NCBI] 6.16454e-06
NGF [NCBI] 4.82885e-06
HPRT1 [NCBI] 3.6255e-06
XDH [NCBI] 3.3123e-06
IL2 [NCBI] 2.49961e-06
G6PD [NCBI] 2.31306e-06
ITPA [NCBI] 1.91687e-06
NEIL1 [NCBI] 1.84879e-06
GFAP [NCBI] 1.73397e-06
NP [NCBI] 1.72197e-06
GCH1 [NCBI] 1.66797e-06
PTH [NCBI] 1.45638e-06
XRCC1 [NCBI] 1.27464e-06
SOD1 [NCBI] 9.32142e-07
DHFR [NCBI] 9.14759e-07
LIF [NCBI] 8.67592e-07
AVP [NCBI] 6.8966e-07
EPO [NCBI] 6.7928e-07
TH [NCBI] 6.49404e-07
ACHE [NCBI] 6.22947e-07
EGF [NCBI] 3.90537e-07




OMIM


OMIM Link Information
gain
01
storage pool platelet disease [NCBI] 0.00448991
LNS [NCBI] 0.00108146
HPRT1 [NCBI] 0.000726833
xanthinuria, type i [NCBI] 0.00066561
XDH [NCBI] 0.00061104
gout, hprt-related [NCBI] 0.000416623
phosphoribosylpyrophosphate synthetase superactivity [NCBI] 0.000337658
hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase [NCBI] 0.000178139
APRT [NCBI] 0.000118648
hypouricemia, renal [NCBI] 9.61622e-05
ED1 [NCBI] 7.92656e-05
ADA [NCBI] 7.77894e-05
FPGS [NCBI] 7.53779e-05
glycogen storage disease vii [NCBI] 7.30923e-05
lymphoma, non-hodgkin, familial [NCBI] 6.58077e-05
AMPD1 [NCBI] 4.61643e-05
MJD [NCBI] 4.50214e-05
TYMS [NCBI] 4.00666e-05
NP [NCBI] 3.60128e-05
G6PD [NCBI] 2.49563e-05
CAT [NCBI] 2.44347e-05
ITPA [NCBI] 2.22665e-05
ENO1 [NCBI] 2.12655e-05
ALDOA [NCBI] 2.12655e-05
TK1 [NCBI] 1.96994e-05
PGK1 [NCBI] 1.47139e-05
IL2 [NCBI] 1.29838e-05
MTR [NCBI] 1.27953e-05
EGF [NCBI] 1.10104e-05
NGFB [NCBI] 5.13138e-06
LCAT [NCBI] 4.63088e-06
CYP1A1 [NCBI] 3.6078e-06
ALB [NCBI] 3.28266e-06
ACHE [NCBI] 1.1083e-06
AVP [NCBI] 8.77038e-07
TH [NCBI] 7.41439e-07
DHFR [NCBI] 6.77109e-07
GFAP [NCBI] 5.72931e-07
EPO [NCBI] 3.78276e-07
PTH [NCBI] 1.60766e-07




Database Center for Life Science