Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	von Willebrand Diseases	[NCBI]

Gene	Link	Information Gain
VWF	[NCBI]	0.00693944
ADAMTS13	[NCBI]	0.000185389
GP1BA	[NCBI]	5.97169e-05
F8	[NCBI]	5.2929e-05
GP5	[NCBI]	1.85373e-05
A1BG	[NCBI]	1.47434e-05
GP1BB	[NCBI]	1.44694e-05
GP9	[NCBI]	1.26734e-05
ANO2	[NCBI]	8.87836e-06
PDIA4	[NCBI]	7.86388e-06
SPZ1	[NCBI]	7.23348e-06
ITGA2B	[NCBI]	7.18403e-06
PF4	[NCBI]	7.0912e-06
LRPAP1	[NCBI]	5.36428e-06
ITGAL	[NCBI]	4.84762e-06
LAMB1	[NCBI]	4.78546e-06
PDIA3	[NCBI]	4.66779e-06
CALR	[NCBI]	4.66779e-06
FURIN	[NCBI]	4.50581e-06
ABO	[NCBI]	4.40615e-06
RAB27A	[NCBI]	3.80791e-06
HSPA5	[NCBI]	3.62013e-06
CPB2	[NCBI]	3.56223e-06
HSP90B1	[NCBI]	3.40048e-06
LRP1	[NCBI]	3.37509e-06
MYH9	[NCBI]	2.88469e-06
F2	[NCBI]	2.50462e-06
PLG	[NCBI]	1.91217e-06
SERPINA1	[NCBI]	1.57567e-06
SELPLG	[NCBI]	1.41061e-06
CFTR	[NCBI]	1.1258e-06
ITGB3	[NCBI]	1.10479e-06
BCR	[NCBI]	4.20964e-07
PTK2	[NCBI]	3.85453e-07
SERPINE1	[NCBI]	3.78971e-07
F5	[NCBI]	2.5765e-07
PLAUR	[NCBI]	3.10205e-08

OMIM	Link	Information gain
von willebrand disease	[NCBI]	0.00822095
von willebrand disease, recessive form	[NCBI]	0.00151533
pseudo-von willebrand disease	[NCBI]	0.00100305
storage pool platelet disease	[NCBI]	0.000847142
GPS	[NCBI]	0.000685
HHT	[NCBI]	0.000390772
hemophilia a	[NCBI]	0.000205109
GP1BA	[NCBI]	0.000185631
giant platelet syndrome	[NCBI]	0.000152498
hemophilia a with vascular abnormality	[NCBI]	0.00012396
B4GALNT2	[NCBI]	0.000121015
thrombocytopenic purpura, autoimmune	[NCBI]	0.000106076
von willebrand disease, x-linked form	[NCBI]	0.000101495
glanzmann thrombasthenia, autosomal dominant	[NCBI]	0.000101495
factor viii deficiency	[NCBI]	9.30209e-05
factor xii deficiency	[NCBI]	6.14841e-05
glycogen storage disease ib	[NCBI]	5.31095e-05
PF4	[NCBI]	4.12969e-05
LRP1	[NCBI]	3.95781e-05
fabry disease	[NCBI]	3.12492e-05
XIST	[NCBI]	3.06531e-05
PKD1	[NCBI]	1.38049e-05
BCR	[NCBI]	8.0072e-06
GIP	[NCBI]	6.95389e-06
ACE	[NCBI]	6.55751e-06
SLE	[NCBI]	1.17338e-06