Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Erythrocyte Deformability	[NCBI]

Gene	Link	Information Gain
DHS	[NCBI]	0.000305671
IGAN	[NCBI]	6.3554e-05
EPB41L2	[NCBI]	4.14941e-05
EPB41L1	[NCBI]	3.50887e-05
SPTA1	[NCBI]	1.62907e-05
SLC4A1	[NCBI]	1.10576e-05
EPO	[NCBI]	1.01121e-05
ACHE	[NCBI]	9.91716e-06
SPTB	[NCBI]	9.53433e-06
NOS3	[NCBI]	6.65558e-06
EPB41	[NCBI]	5.76506e-06
G6PD	[NCBI]	5.48163e-06
AMPD3	[NCBI]	3.24272e-06
EPB49	[NCBI]	2.99873e-06
EPB42	[NCBI]	2.9059e-06
SLC16A1	[NCBI]	2.82886e-06
GGT1	[NCBI]	2.66258e-06
ANK1	[NCBI]	2.60859e-06
RHAG	[NCBI]	2.58728e-06
STOM	[NCBI]	2.52878e-06
GPI	[NCBI]	2.28119e-06
AQP1	[NCBI]	2.27071e-06
CD47	[NCBI]	2.13718e-06
PTH	[NCBI]	2.00351e-06
ADCYAP1	[NCBI]	1.8784e-06
PIH	[NCBI]	1.74641e-06
INS	[NCBI]	1.60047e-06
ADA	[NCBI]	1.36981e-06
ACE	[NCBI]	1.25372e-06
TLR4	[NCBI]	1.10299e-06
CAT	[NCBI]	1.05411e-06
VWF	[NCBI]	9.01825e-07
CFTR	[NCBI]	7.37026e-07

OMIM	Link	Information gain
DHS	[NCBI]	0.00180262
red cell phospholipid defect with hemolysis	[NCBI]	0.00103894
SPTA1	[NCBI]	0.000320542
HPP	[NCBI]	0.000274822
dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema	[NCBI]	0.000145472
EPO	[NCBI]	5.97201e-05
ACHE	[NCBI]	5.51021e-05
apnea, obstructive sleep	[NCBI]	5.36303e-05
SLC4A1	[NCBI]	4.96075e-05
temporal arteritis	[NCBI]	4.92088e-05
EPB72	[NCBI]	3.42765e-05
G6PD	[NCBI]	3.26356e-05
EPB42	[NCBI]	2.89112e-05
EPB41	[NCBI]	2.83022e-05
SPTB	[NCBI]	2.61447e-05
CF	[NCBI]	2.1774e-05
GPI	[NCBI]	1.24326e-05
XDH	[NCBI]	7.82017e-06
HBB	[NCBI]	6.8022e-06
ADA	[NCBI]	6.09319e-06
RA	[NCBI]	5.84892e-06
PTH	[NCBI]	4.64525e-06
CFTR	[NCBI]	3.04334e-06
CAT	[NCBI]	3.03018e-06