Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	IgA Deficiency	[NCBI]

Gene	Link	Information Gain
IGAD1	[NCBI]	0.000854821
IGAN	[NCBI]	8.93865e-05
TNFRSF13B	[NCBI]	8.88854e-05
TNFSF13B	[NCBI]	2.68412e-05
TNFSF13	[NCBI]	1.99894e-05
NBN	[NCBI]	1.45168e-05
BTK	[NCBI]	1.41968e-05
HLA-B	[NCBI]	1.33352e-05
TNF	[NCBI]	1.23859e-05
MSH5	[NCBI]	1.18236e-05
HLA-DQB1	[NCBI]	1.17318e-05
IL10	[NCBI]	1.10086e-05
HLA-DRA	[NCBI]	9.54036e-06
TNFRSF13C	[NCBI]	9.06198e-06
TGM2	[NCBI]	7.91249e-06
AFP	[NCBI]	7.89095e-06
MAP3K14	[NCBI]	7.79497e-06
PTPN22	[NCBI]	6.95078e-06
TAP2	[NCBI]	6.62913e-06
AMBP	[NCBI]	6.26429e-06
TAP1	[NCBI]	6.17462e-06
HLA-DQA1	[NCBI]	5.90773e-06
HLA-A	[NCBI]	5.86635e-06
HLA-DRB1	[NCBI]	4.05243e-06
IL6	[NCBI]	3.77777e-06

OMIM	Link	Information gain
IGAD1	[NCBI]	0.010087
CVID	[NCBI]	0.00269164
ocular motor apraxia	[NCBI]	0.00056504
pulmonary alveolar proteinosis, acquired	[NCBI]	0.000528242
CD	[NCBI]	0.000389034
TNFRSF13B	[NCBI]	0.000210686
IGAD2	[NCBI]	0.000187762
HIGM1	[NCBI]	0.000179672
ataxia-telangiectasia with generalized skin pigmentation and early death	[NCBI]	0.000116222
MSH5	[NCBI]	9.09049e-05
BTK	[NCBI]	8.59254e-05
CHH	[NCBI]	8.53892e-05
IGHG2	[NCBI]	7.71252e-05
IGLC1	[NCBI]	6.60373e-05
IFNG	[NCBI]	4.96058e-05
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant	[NCBI]	4.72104e-05
BLM	[NCBI]	3.08448e-05
MBL2	[NCBI]	2.67493e-05
AFP	[NCBI]	2.44558e-05
RA	[NCBI]	2.43933e-05
TNF	[NCBI]	2.05968e-05
TTR	[NCBI]	1.82998e-05
SLE	[NCBI]	1.38342e-05
AT	[NCBI]	1.01137e-05
CEACAM5	[NCBI]	2.60153e-06