Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Conjunctivitis	[NCBI]

Gene	Link	Information Gain
WG	[NCBI]	0.000283087
PLG	[NCBI]	9.86067e-05
NLRP3	[NCBI]	1.6612e-05
GALNT6	[NCBI]	1.50142e-05
GALNT4	[NCBI]	1.41158e-05
TGFB1	[NCBI]	1.36658e-05
IL4	[NCBI]	1.2813e-05
GALNT1	[NCBI]	1.27529e-05
GALNT2	[NCBI]	1.27529e-05
NFKBIZ	[NCBI]	1.27529e-05
SAMD9	[NCBI]	1.24654e-05
GALNT3	[NCBI]	1.10868e-05
ADA	[NCBI]	1.07867e-05
FCER1A	[NCBI]	9.55041e-06
SELL	[NCBI]	8.91259e-06
S100A12	[NCBI]	8.8473e-06
SELP	[NCBI]	7.8022e-06
TNFRSF1A	[NCBI]	7.13546e-06
SELE	[NCBI]	7.12377e-06
IL4R	[NCBI]	6.885e-06
IL13	[NCBI]	6.74889e-06
HLA-C	[NCBI]	6.37346e-06
HLA-A	[NCBI]	5.53199e-06
LAMB3	[NCBI]	5.4352e-06
TFF1	[NCBI]	5.15647e-06
HLA-B	[NCBI]	5.12427e-06
CD86	[NCBI]	5.00467e-06
TLR2	[NCBI]	4.83565e-06
CTGF	[NCBI]	4.70424e-06
TNF	[NCBI]	3.33246e-06
IL1RN	[NCBI]	3.15273e-06
FASLG	[NCBI]	2.56852e-06
NGF	[NCBI]	2.53635e-06

OMIM	Link	Information gain
OCP	[NCBI]	0.00157111
plasminogen deficiency, type i	[NCBI]	0.00100735
epidermolysis bullosa inversa dystrophica	[NCBI]	0.00098052
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging	[NCBI]	0.000807657
PLG	[NCBI]	0.000622969
amyloidosis of gingiva and conjunctiva, with mental retardation	[NCBI]	0.000126428
allergic bronchopulmonary aspergillosis	[NCBI]	0.000103962
NFTC	[NCBI]	9.54859e-05
severe cutaneous adverse reaction, susceptibility to	[NCBI]	7.07024e-05
SAMD9	[NCBI]	6.96426e-05
RA	[NCBI]	5.5502e-05
BOR1	[NCBI]	5.44947e-05
FCAS	[NCBI]	5.25829e-05
periodic fever, familial, autosomal dominant	[NCBI]	5.21391e-05
HLA-A	[NCBI]	4.50765e-05
SLS	[NCBI]	3.96058e-05
ADA	[NCBI]	3.94975e-05
MCP	[NCBI]	3.51633e-05
SLE	[NCBI]	3.45903e-05
CTGF	[NCBI]	2.08105e-05
lymphoma, non-hodgkin, familial	[NCBI]	7.26754e-06
NGFB	[NCBI]	4.75806e-06
TNF	[NCBI]	4.7459e-06