Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Ristocetin	[NCBI]

Gene	Link	Information Gain
VWF	[NCBI]	0.000461844
GP1BA	[NCBI]	2.63639e-05
GP1BB	[NCBI]	1.13454e-05
GP9	[NCBI]	5.08172e-06
ADAMTS13	[NCBI]	4.27124e-06
A1BG	[NCBI]	3.21702e-06
PF4	[NCBI]	2.91647e-06
ITGA2B	[NCBI]	2.19686e-06
SCUBE1	[NCBI]	1.82319e-06
F8	[NCBI]	1.812e-06
GP5	[NCBI]	1.57494e-06
FUT8	[NCBI]	1.19419e-06
COL1A2	[NCBI]	1.02434e-06
COL1A1	[NCBI]	8.59127e-07
HBB	[NCBI]	7.94605e-07
PLEK	[NCBI]	7.2662e-07
BTK	[NCBI]	6.58934e-07
MAPK1	[NCBI]	6.2785e-07
CTSG	[NCBI]	5.94876e-07
NOS3	[NCBI]	3.57066e-07
NOS2	[NCBI]	3.45889e-07

OMIM	Link	Information gain
giant platelet syndrome	[NCBI]	0.00102284
pseudo-von willebrand disease	[NCBI]	0.00082013
von willebrand disease	[NCBI]	0.000697947
factor ix and factor xi, combined deficiency of	[NCBI]	0.000185453
von willebrand disease, x-linked form	[NCBI]	0.000153868
factors viii, ix and xi, combined deficiency of	[NCBI]	0.000153868
factor viii deficiency	[NCBI]	0.000141951
von willebrand disease, recessive form	[NCBI]	0.000107087
MHA	[NCBI]	9.62935e-05
bartter syndrome, type 3	[NCBI]	8.65092e-05
GP1BA	[NCBI]	5.93976e-05
PF4	[NCBI]	4.91129e-05
GP1BB	[NCBI]	3.28078e-05
HS	[NCBI]	2.31791e-05
hemophilia a	[NCBI]	1.68275e-05