Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Oxalates	[NCBI]

Gene	Link	Information Gain
AGXT2L1	[NCBI]	3.58432e-05
SLC26A6	[NCBI]	1.63229e-05
UMOD	[NCBI]	1.04986e-05
PTH	[NCBI]	6.48506e-06
PLN	[NCBI]	6.39238e-06
GRHPR	[NCBI]	5.99677e-06
AGXT	[NCBI]	3.833e-06
SLC26A3	[NCBI]	3.68564e-06
SPINT2	[NCBI]	2.88587e-06
AGXT2	[NCBI]	2.26702e-06
SLC26A9	[NCBI]	2.15035e-06
CASP3	[NCBI]	2.1411e-06
TF	[NCBI]	2.11099e-06
KHK	[NCBI]	1.79145e-06
SLC25A11	[NCBI]	1.65321e-06
ATP2A1	[NCBI]	1.64357e-06
SLC26A2	[NCBI]	1.56256e-06
PTPRN2	[NCBI]	1.55228e-06
SLC22A12	[NCBI]	1.51765e-06
RYR1	[NCBI]	1.43243e-06
SLC4A1	[NCBI]	1.32454e-06
PTPRN	[NCBI]	1.26919e-06
CS	[NCBI]	1.13448e-06
SLC9A3	[NCBI]	1.05271e-06
ITPR1	[NCBI]	1.03726e-06
EGR1	[NCBI]	9.57666e-07
ALB	[NCBI]	9.56952e-07
EGF	[NCBI]	8.6478e-07
COMT	[NCBI]	8.40842e-07
G6PD	[NCBI]	8.29665e-07
ADA	[NCBI]	7.99549e-07
CD68	[NCBI]	7.53995e-07
IL6	[NCBI]	7.3469e-07
CASP9	[NCBI]	7.08431e-07
TLR4	[NCBI]	6.98015e-07
TGFB1	[NCBI]	5.77034e-07
CFTR	[NCBI]	4.90672e-07
PTGS2	[NCBI]	4.35698e-07

OMIM	Link	Information gain
nephrolithiasis, calcium oxalate	[NCBI]	0.0219823
hyperoxaluria, primary, type i	[NCBI]	0.00305847
hyperoxaluria, primary, type ii	[NCBI]	0.000425549
glycinuria with or without oxalate urolithiasis	[NCBI]	0.000126032
hydroxyprolinemia	[NCBI]	0.000120283
hypouricemia, renal	[NCBI]	9.52902e-05
SPP1	[NCBI]	8.42497e-05
solute carrier family 26 (anion transporter), member 6: slc26a6	[NCBI]	8.23205e-05
GCE	[NCBI]	7.92037e-05
PTH	[NCBI]	6.77324e-05
AGXT	[NCBI]	6.7372e-05
wilson disease	[NCBI]	5.17003e-05
TF	[NCBI]	2.42113e-05
TLR4	[NCBI]	1.06292e-05
ALB	[NCBI]	1.03467e-05
COMT	[NCBI]	9.26534e-06
CF	[NCBI]	8.38977e-06
ADA	[NCBI]	6.81652e-06
G6PD	[NCBI]	6.79861e-06
EGF	[NCBI]	2.18527e-06