Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Purpura, Thrombocytopenic	[NCBI]

Gene	Link	Information Gain
VWF	[NCBI]	8.96393e-05
ADAMTS13	[NCBI]	8.87308e-05
MSLN	[NCBI]	1.57961e-05
PF4	[NCBI]	1.29611e-05
PIH	[NCBI]	1.25673e-05
EPO	[NCBI]	1.22733e-05
TROVE2	[NCBI]	1.16734e-05
CD109	[NCBI]	1.09267e-05
GP6	[NCBI]	1.03859e-05
CD244	[NCBI]	9.26791e-06
CD68	[NCBI]	8.42903e-06
ITGA2B	[NCBI]	7.27826e-06
CD40LG	[NCBI]	6.86607e-06
F5	[NCBI]	4.32813e-06
ADA	[NCBI]	3.93186e-06
FASLG	[NCBI]	2.31334e-06
PCNA	[NCBI]	2.04354e-06

OMIM	Link	Information gain
thrombocytopenic purpura, autoimmune	[NCBI]	0.0261292
thrombocytopenia, autosomal recessive	[NCBI]	0.00172954
storage pool platelet disease	[NCBI]	0.00143921
thrombocytopenia-absent radius syndrome	[NCBI]	0.00109535
RA	[NCBI]	0.000887221
GPS	[NCBI]	0.000432047
hemophagocytic lymphohistiocytosis, familial, 1	[NCBI]	0.000372668
SLE	[NCBI]	0.000265528
thrombasthenia of glanzmann and naegeli	[NCBI]	0.000257193
giant platelet syndrome	[NCBI]	0.000150239
THC1	[NCBI]	0.000144794
THC2	[NCBI]	0.00012757
ITGB3	[NCBI]	0.000101603
MG	[NCBI]	7.74588e-05
HPA-2	[NCBI]	7.59186e-05
autoimmune disease	[NCBI]	7.32448e-05
LNPEP	[NCBI]	6.73416e-05
splenomegaly syndrome with splenic germinal center hypoplasia and reduced circulating t-helper cells	[NCBI]	6.35149e-05
thrombocytopenia, cyclic	[NCBI]	6.35149e-05
hemangioma-thrombocytopenia syndrome	[NCBI]	6.07347e-05
PF4	[NCBI]	5.7744e-05
ETS1	[NCBI]	5.39023e-05
MME	[NCBI]	5.19102e-05
GP1BA	[NCBI]	5.13263e-05
ITGA2B	[NCBI]	5.13263e-05
EPO	[NCBI]	4.58642e-05
WAS	[NCBI]	4.08287e-05
KITLG	[NCBI]	3.88825e-05
protein c deficiency, congenital thrombotic disease due to	[NCBI]	3.84125e-05
sea-blue histiocyte disease	[NCBI]	3.23956e-05
lymphoma, non-hodgkin, familial	[NCBI]	2.58042e-05
TTP	[NCBI]	1.92232e-05
ADA	[NCBI]	1.41129e-05
F3	[NCBI]	1.21141e-05
WAS	[NCBI]	9.01292e-06
gaucher disease, type i	[NCBI]	5.29434e-06
PCNA	[NCBI]	4.55026e-06
CVID	[NCBI]	2.86829e-06
DBA	[NCBI]	1.70345e-06