Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hematoma	[NCBI]

Gene	Link	Information Gain
FOP	[NCBI]	0.000271232
F8	[NCBI]	7.01407e-05
VWF	[NCBI]	1.86896e-05
KCNK6	[NCBI]	1.28157e-05
TFPI	[NCBI]	1.26005e-05
SERPINF2	[NCBI]	1.0804e-05
C3AR1	[NCBI]	8.44152e-06
S100B	[NCBI]	8.35442e-06
NOTCH4	[NCBI]	8.16697e-06
MBP	[NCBI]	7.97139e-06
PROCR	[NCBI]	7.88695e-06
TFPI2	[NCBI]	7.37104e-06
MPO	[NCBI]	6.75088e-06
IGF2	[NCBI]	5.90288e-06
CYP2C19	[NCBI]	5.70206e-06
ALK	[NCBI]	5.21347e-06
WAS	[NCBI]	5.17856e-06
SLC2A1	[NCBI]	4.96046e-06
UMOD	[NCBI]	4.93418e-06
APP	[NCBI]	4.81222e-06
BMP2	[NCBI]	4.57751e-06
SERPINE1	[NCBI]	4.56855e-06
CST3	[NCBI]	3.96632e-06
TRH	[NCBI]	3.57287e-06
TG	[NCBI]	3.4996e-06
TNF	[NCBI]	2.86119e-06
GFAP	[NCBI]	2.35967e-06
VEGFA	[NCBI]	2.18121e-06
PRL	[NCBI]	2.07508e-06
EGF	[NCBI]	1.36072e-06

OMIM	Link	Information gain
d-glyceric acidemia	[NCBI]	0.000840405
fatty metamorphosis of viscera	[NCBI]	0.000817902
amyloidosis vi	[NCBI]	0.000578916
klippel-trenaunay-weber syndrome	[NCBI]	0.000459121
plasmin inhibitor deficiency	[NCBI]	0.00020183
coracoclavicular joint, anomalous	[NCBI]	0.000127341
ovarian teratoma	[NCBI]	9.08966e-05
KRT8	[NCBI]	5.69272e-05
pheochromocytoma	[NCBI]	5.48965e-05
PLAT	[NCBI]	5.23317e-05
TFPI	[NCBI]	5.20476e-05
thrombocytopenic purpura, autoimmune	[NCBI]	5.0031e-05
glioma of brain, familial	[NCBI]	4.47367e-05
TFPI2	[NCBI]	4.42512e-05
F13A1	[NCBI]	4.16929e-05
FOP	[NCBI]	4.10873e-05
factor x deficiency	[NCBI]	4.07395e-05
FMF	[NCBI]	4.01186e-05
factor v deficiency	[NCBI]	3.51727e-05
F3	[NCBI]	3.43205e-05
RA	[NCBI]	2.73654e-05
CPI	[NCBI]	2.6293e-05
MBP	[NCBI]	2.62825e-05
PJS	[NCBI]	2.50918e-05
dystrophia myotonica 1	[NCBI]	2.41134e-05
WAS	[NCBI]	2.02669e-05
MPO	[NCBI]	2.0063e-05
polycystic kidneys	[NCBI]	1.70658e-05
FA	[NCBI]	1.16597e-05
TG	[NCBI]	1.05026e-05
GFAP	[NCBI]	4.8048e-06
TNF	[NCBI]	4.20491e-06
APC	[NCBI]	3.94837e-06
PRL	[NCBI]	3.35868e-06
VEGF	[NCBI]	3.05795e-06
MG	[NCBI]	1.72373e-06
SLE	[NCBI]	1.30317e-06
EGF	[NCBI]	1.02182e-06