Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Protein C Deficiency	[NCBI]

Gene	Link	Information Gain
PROC	[NCBI]	0.000657876
F5	[NCBI]	0.000100884
F2	[NCBI]	8.59019e-05
MTHFR	[NCBI]	3.08535e-05
PROCR	[NCBI]	2.61795e-05
GGCX	[NCBI]	2.24853e-05
ONECUT1	[NCBI]	2.12878e-05
PAFAH1B2	[NCBI]	1.36418e-05
HNF1B	[NCBI]	1.08997e-05
HNF1A	[NCBI]	1.0608e-05
PROZ	[NCBI]	9.03994e-06
F10	[NCBI]	8.55695e-06
PROS1	[NCBI]	7.51148e-06
F7	[NCBI]	5.85872e-06
PLG	[NCBI]	5.56722e-06
VWF	[NCBI]	4.91927e-06
NQO1	[NCBI]	4.6213e-06
PF4	[NCBI]	4.21765e-06
PAH	[NCBI]	4.20864e-06
F8	[NCBI]	3.99041e-06
TTR	[NCBI]	3.61504e-06
SERPINE1	[NCBI]	3.51912e-06
PTGS1	[NCBI]	3.04101e-06

OMIM	Link	Information gain
protein c deficiency, congenital thrombotic disease due to	[NCBI]	0.00281525
PEE1	[NCBI]	0.000860596
factor v deficiency	[NCBI]	0.000255519
thrombophilia due to deficiency of activated protein c cofactor	[NCBI]	0.000111537
legg-calve-perthes disease	[NCBI]	9.94045e-05
vitamin k-dependent clotting factors, combined deficiency of, 1	[NCBI]	9.37095e-05
LPA	[NCBI]	9.07617e-05
homocysteinemia	[NCBI]	8.10551e-05
PROCR	[NCBI]	7.76045e-05
CDG1A	[NCBI]	7.30194e-05
PCI	[NCBI]	7.17925e-05
antithrombin iii deficiency	[NCBI]	5.7595e-05
HCF2	[NCBI]	5.01906e-05
GGCX	[NCBI]	4.37739e-05
PI	[NCBI]	3.83165e-05
PROS1	[NCBI]	3.29388e-05
FMF	[NCBI]	3.22336e-05
F2	[NCBI]	2.89235e-05
factor vii deficiency	[NCBI]	2.8522e-05
PLG	[NCBI]	1.82761e-05
ACE	[NCBI]	1.24185e-05
PF4	[NCBI]	1.03202e-05
TTR	[NCBI]	6.30902e-06
CF	[NCBI]	2.32532e-06
SLE	[NCBI]	1.36693e-08