Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Glycolates	[NCBI]

Gene	Link	Information Gain
AGXT2L1	[NCBI]	1.84494e-05
TDP1	[NCBI]	6.41122e-06
GRHPR	[NCBI]	6.37513e-06
BMP2	[NCBI]	5.06199e-06
PGP	[NCBI]	4.21568e-06
CLIC1	[NCBI]	4.10981e-06
PRKDC	[NCBI]	2.59831e-06
XRCC5	[NCBI]	2.53718e-06
AGXT2	[NCBI]	2.39101e-06
BPGM	[NCBI]	2.08101e-06
TREX1	[NCBI]	1.96008e-06
GSTZ1	[NCBI]	1.9154e-06
AGXT	[NCBI]	1.85001e-06
TPI1	[NCBI]	1.83134e-06
APTX	[NCBI]	1.74049e-06
DCLRE1C	[NCBI]	1.67616e-06
LIG3	[NCBI]	1.62714e-06
CFTR	[NCBI]	1.58293e-06
XRCC6	[NCBI]	1.5356e-06
KRT5	[NCBI]	1.48672e-06
ETS2	[NCBI]	1.47697e-06
APEX1	[NCBI]	1.44971e-06
CYP1B1	[NCBI]	1.35801e-06
WRN	[NCBI]	1.27013e-06
DCT	[NCBI]	1.24696e-06
IBSP	[NCBI]	1.13949e-06
BMP4	[NCBI]	1.1268e-06
FOLR1	[NCBI]	1.03492e-06
NFKB1	[NCBI]	1.00907e-06
G6PD	[NCBI]	9.51985e-07
CDK2	[NCBI]	8.74117e-07
CASP9	[NCBI]	8.29767e-07
AFP	[NCBI]	7.25361e-07
AR	[NCBI]	6.89107e-07
AVP	[NCBI]	6.72723e-07
PCNA	[NCBI]	6.44307e-07
CDKN1A	[NCBI]	5.82424e-07
CASP3	[NCBI]	5.46523e-07
PTH	[NCBI]	5.29909e-07
TNF	[NCBI]	3.40992e-07

OMIM	Link	Information gain
hyperoxaluria, primary, type i	[NCBI]	0.000857337
hyperoxaluria, primary, type ii	[NCBI]	0.000299241
hydroxyprolinemia	[NCBI]	0.000139291
PHA2	[NCBI]	0.000107087
adrenoleukodystrophy, autosomal neonatal form	[NCBI]	8.82258e-05
WRN	[NCBI]	7.81184e-05
AGXT	[NCBI]	7.12602e-05
PGP	[NCBI]	6.52657e-05
diphosphoglycerate mutase deficiency of erythrocyte	[NCBI]	3.26603e-05
CFTR	[NCBI]	2.01972e-05
CDK2	[NCBI]	1.65925e-05
SERPINA6	[NCBI]	1.61529e-05
SPP1	[NCBI]	9.87248e-06
G6PD	[NCBI]	8.50765e-06
AR	[NCBI]	5.0708e-06
VEGF	[NCBI]	5.01227e-06
AFP	[NCBI]	5.0046e-06
PCNA	[NCBI]	3.71845e-06
AVP	[NCBI]	3.27007e-06
PTH	[NCBI]	1.99772e-06
TNF	[NCBI]	3.15154e-07
CF	[NCBI]	7.87444e-08