Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hypoprothrombinemias	[NCBI]

Gene	Link	Information Gain
F2	[NCBI]	9.15672e-05
VKORC1	[NCBI]	3.27244e-05
GGCX	[NCBI]	2.73408e-05
F10	[NCBI]	1.0946e-05
ATP8B1	[NCBI]	1.0106e-05
TPMT	[NCBI]	9.12275e-06
TTR	[NCBI]	5.94674e-06
F5	[NCBI]	5.603e-06
PTGS2	[NCBI]	2.60775e-06

OMIM	Link	Information gain
factor x deficiency	[NCBI]	0.00130991
scott syndrome	[NCBI]	0.0010375
F2	[NCBI]	0.000962934
vitamin k-dependent clotting factors, combined deficiency of, 1	[NCBI]	0.00072148
F8FD9	[NCBI]	0.000120084
factor vii and factor viii, combined deficiency of	[NCBI]	0.000111604
hyperpipecolatemia	[NCBI]	9.37095e-05
F5F8D	[NCBI]	8.4187e-05
factor vii deficiency	[NCBI]	8.06276e-05
PFIC1	[NCBI]	6.90237e-05
PGL1	[NCBI]	6.52872e-05
GGCX	[NCBI]	4.8574e-05
ATP8B1	[NCBI]	4.76717e-05
SLE	[NCBI]	4.24705e-05
TPMT	[NCBI]	3.36627e-05
antithrombin iii deficiency	[NCBI]	2.66442e-05
TTR	[NCBI]	1.01699e-05