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01 Kidney Calculi [NCBI]


Gene


Gene Link Information
Gain
01
UMOD [NCBI] 0.000600386
VUR [NCBI] 0.000422915
APRT [NCBI] 0.000190001
PTH [NCBI] 0.000160549
CLCN5 [NCBI] 0.000134648
SPINT2 [NCBI] 9.17495e-05
IGAN [NCBI] 6.51999e-05
VDR [NCBI] 6.49445e-05
SLC7A9 [NCBI] 6.2571e-05
SLC13A2 [NCBI] 4.97588e-05
AMBP [NCBI] 4.97297e-05
AGXT2L1 [NCBI] 3.5072e-05
SLC34A1 [NCBI] 3.23916e-05
GRHPR [NCBI] 2.74452e-05
CASR [NCBI] 2.39336e-05
ZNF365 [NCBI] 2.3383e-05
SLC22A12 [NCBI] 2.21626e-05
FGF23 [NCBI] 2.05665e-05
SPP1 [NCBI] 1.62235e-05
XDH [NCBI] 1.28361e-05
SLC3A1 [NCBI] 1.22071e-05
TFF1 [NCBI] 1.13057e-05
REG1A [NCBI] 1.05929e-05
SLC34A3 [NCBI] 9.14101e-06
SLC17A2 [NCBI] 8.89534e-06
SLC9A3R1 [NCBI] 8.31835e-06
SLC22A18 [NCBI] 8.31835e-06
TRPV6 [NCBI] 7.54468e-06
AGXT [NCBI] 6.61168e-06
CALCR [NCBI] 6.55293e-06
ST6GAL1 [NCBI] 6.33647e-06
CA2 [NCBI] 6.1906e-06
CDKN2D [NCBI] 6.14466e-06
CLCNKB [NCBI] 5.70816e-06
MS [NCBI] 5.58416e-06
LOX [NCBI] 5.57397e-06
CDC73 [NCBI] 4.91703e-06
SLC12A1 [NCBI] 4.83251e-06
CLCN1 [NCBI] 4.75213e-06
B2M [NCBI] 4.33867e-06
MGP [NCBI] 3.68595e-06
PLAU [NCBI] 3.67589e-06
IBSP [NCBI] 3.3594e-06
CD44 [NCBI] 2.94673e-06
HSPB1 [NCBI] 2.72753e-06
SDC1 [NCBI] 2.53716e-06
ALB [NCBI] 2.2461e-06
PKD1 [NCBI] 2.04846e-06
F2 [NCBI] 1.84277e-06
CST3 [NCBI] 1.24058e-06
PCNA [NCBI] 1.23261e-06
ADA [NCBI] 1.21283e-06
CFTR [NCBI] 9.47994e-07
TLR4 [NCBI] 8.4753e-07
CAT [NCBI] 7.42676e-07
HGF [NCBI] 4.10583e-07
EGF [NCBI] 3.80564e-07
EPO [NCBI] 1.50242e-07
PTGS2 [NCBI] 9.01141e-09




OMIM


OMIM Link Information
gain
01
nephrolithiasis, calcium oxalate [NCBI] 0.00494549
APRT [NCBI] 0.000937602
dent disease 1 [NCBI] 0.000767351
leukonychia totalis [NCBI] 0.000715905
XRN [NCBI] 0.000662121
hyperoxaluria, primary, type i [NCBI] 0.000544084
PTH [NCBI] 0.000531807
HCA2 [NCBI] 0.000489687
SPP1 [NCBI] 0.000485792
alport syndrome, autosomal dominant [NCBI] 0.000394467
UMOD [NCBI] 0.000359802
CLCN5 [NCBI] 0.000293697
uric acid nephrolithiasis, susceptibility to [NCBI] 0.000235159
hypophosphatemic rickets, x-linked recessive [NCBI] 0.000180644
hyperoxaluria, primary, type ii [NCBI] 0.000173295
VDR [NCBI] 0.000167403
hypouricemia, renal [NCBI] 0.000150714
proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis [NCBI] 0.000147626
xanthinuria, type i [NCBI] 0.000137595
renal tubular acidosis, distal, autosomal dominant [NCBI] 0.000137595
wilson disease [NCBI] 0.000130756
tachycardia, hypertension, microphthalmia, and hyperglycinuria [NCBI] 0.000117451
CASR [NCBI] 0.000102495
glycogen storage disease i [NCBI] 8.98252e-05
hypomagnesemia, renal, with ocular involvement [NCBI] 8.65192e-05
glycinuria with or without oxalate urolithiasis [NCBI] 8.10223e-05
UOX [NCBI] 7.36852e-05
steatocystoma multiplex [NCBI] 7.36852e-05
ZNF365 [NCBI] 6.89903e-05
gout, hprt-related [NCBI] 6.867e-05
RA [NCBI] 6.31403e-05
hyperprolinemia, type i [NCBI] 6.0439e-05
phosphoribosylpyrophosphate synthetase superactivity [NCBI] 5.59825e-05
FGF23 [NCBI] 5.50346e-05
SLE [NCBI] 5.31959e-05
CSID [NCBI] 5.10224e-05
GACI [NCBI] 5.10224e-05
solute carrier family 26 (anion transporter), member 6: slc26a6 [NCBI] 5.00273e-05
alkaptonuria [NCBI] 4.72588e-05
adenylyl cyclase, soluble [NCBI] 4.6659e-05
REG1A [NCBI] 4.6659e-05
SLC34A3 [NCBI] 4.6659e-05
SLC34A1 [NCBI] 4.41569e-05
HPRT1 [NCBI] 4.07781e-05
GRHPR [NCBI] 4.05099e-05
polycystic kidneys [NCBI] 3.66932e-05
XDH [NCBI] 3.47378e-05
SLC7A9 [NCBI] 3.40598e-05
LNS [NCBI] 3.39594e-05
SDC2 [NCBI] 3.38759e-05
AMC [NCBI] 3.3502e-05
AGXT [NCBI] 3.3304e-05
HGD [NCBI] 3.3304e-05
MEN2A [NCBI] 2.95791e-05
PTHR1 [NCBI] 2.83109e-05
TFF1 [NCBI] 2.74835e-05
LOX [NCBI] 2.36355e-05
PXE [NCBI] 1.57534e-05
BWS [NCBI] 1.16245e-05
CF [NCBI] 9.7842e-06
EGF [NCBI] 7.03471e-06
EPO [NCBI] 4.1219e-06
TLR4 [NCBI] 4.07261e-06
F3 [NCBI] 4.00166e-06
ALB [NCBI] 3.75474e-06
HGF [NCBI] 8.94914e-07
PCNA [NCBI] 6.75062e-07
ADA [NCBI] 2.60489e-07
AVP [NCBI] 2.53741e-07
thrombocytopenic purpura, autoimmune [NCBI] 1.43396e-07
NPPA [NCBI] 1.26919e-07
CAT [NCBI] 6.29734e-08




Database Center for Life Science