Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Intestinal Pseudo-Obstruction	[NCBI]

Gene	Link	Information Gain
TRNL1	[NCBI]	0.000287562
SOX10	[NCBI]	2.0516e-05
NOS1	[NCBI]	1.58449e-05
TLX2	[NCBI]	1.35144e-05
VIP	[NCBI]	1.18284e-05
EDN3	[NCBI]	1.06881e-05
MNX1	[NCBI]	1.05717e-05
SLC26A3	[NCBI]	1.03112e-05
DES	[NCBI]	1.00024e-05
FLNA	[NCBI]	9.84815e-06
TLX1	[NCBI]	9.45443e-06
L1CAM	[NCBI]	9.42537e-06
EDNRB	[NCBI]	9.36868e-06
TYMP	[NCBI]	9.28702e-06
PLEC1	[NCBI]	9.01709e-06
PHOX2B	[NCBI]	8.56144e-06
CRH	[NCBI]	7.76887e-06
CP	[NCBI]	7.00652e-06
FAS	[NCBI]	5.98107e-06
CALCA	[NCBI]	4.63287e-06
IL6	[NCBI]	4.18455e-06
PCNA	[NCBI]	2.9887e-06
CFTR	[NCBI]	2.76909e-06

OMIM	Link	Information gain
megaduodenum and/or megacystis	[NCBI]	0.00600518
visceral myopathy, familial, with external ophthalmoplegia	[NCBI]	0.00441496
visceral neuropathy, familial, autosomal recessive	[NCBI]	0.00198068
MGS	[NCBI]	0.00191188
visceral neuropathy, familial, autosomal dominant	[NCBI]	0.00147665
MNGIE	[NCBI]	0.000590684
intestinal pseudoobstruction, neuronal, chronic idiopathic, x-linked	[NCBI]	0.000440442
achalasia, familial esophageal	[NCBI]	0.000379617
SPS	[NCBI]	0.000199197
SLE	[NCBI]	0.000142588
SOX10	[NCBI]	0.000116063
FLNA	[NCBI]	0.000108008
L1CAM	[NCBI]	0.000107464
PCWH	[NCBI]	9.51693e-05
myopathy, myofibrillar, desmin-related	[NCBI]	6.24072e-05
ECGF1	[NCBI]	5.89764e-05
MYH11	[NCBI]	4.94173e-05
DES	[NCBI]	4.68859e-05
VIP	[NCBI]	4.37089e-05
tyrosinemia, type i	[NCBI]	4.06738e-05
HSCR1	[NCBI]	3.63557e-05
RA	[NCBI]	3.28911e-05
CP	[NCBI]	2.872e-05
dystrophia myotonica 1	[NCBI]	2.80488e-05
PCNA	[NCBI]	6.40197e-06
MG	[NCBI]	3.7199e-06