Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Cerebral Arterial Diseases	[NCBI]

Gene	Link	Information Gain
NOTCH3	[NCBI]	9.97281e-05
CST3	[NCBI]	2.86092e-05
ILVBL	[NCBI]	1.78633e-05
AGT	[NCBI]	1.30002e-05
CST2	[NCBI]	1.22815e-05
ACE	[NCBI]	1.08538e-05
MTHFR	[NCBI]	1.01419e-05
NR3C1	[NCBI]	7.47711e-06
JAG1	[NCBI]	7.09702e-06
CYBA	[NCBI]	6.82343e-06
NOTCH1	[NCBI]	6.48753e-06
AGTR1	[NCBI]	6.22825e-06
CXCR3	[NCBI]	6.00361e-06
TGFBR1	[NCBI]	5.97641e-06
F5	[NCBI]	5.06112e-06
PCNA	[NCBI]	2.71775e-06
EGFR	[NCBI]	2.09979e-06

OMIM	Link	Information gain
syringomyelia, isolated	[NCBI]	0.000840405
amyloidosis vi	[NCBI]	0.00080114
CARASIL	[NCBI]	0.000765046
aneurysm, intracranial berry, 1	[NCBI]	0.000583375
CADASIL	[NCBI]	0.000531038
FHM1	[NCBI]	0.00014272
arterial occlusive disease, progressive, with hypertension, heart defects, bone fragility, and brachysyndactyly	[NCBI]	0.00010915
ILVBL	[NCBI]	9.68811e-05
vasculopathy, retinal, with cerebral leukodystrophy	[NCBI]	8.5109e-05
TREX1	[NCBI]	6.45705e-05
NOTCH3	[NCBI]	6.26709e-05
CST3	[NCBI]	5.36558e-05
WBS	[NCBI]	3.05796e-05
NF1	[NCBI]	2.96081e-05
PXE	[NCBI]	2.83744e-05
F3	[NCBI]	1.86684e-05
temporal arteritis	[NCBI]	1.80624e-05
CRH	[NCBI]	1.54055e-05
PWS	[NCBI]	1.28829e-05
PCNA	[NCBI]	1.00931e-05
EGFR	[NCBI]	8.07904e-06
SLE	[NCBI]	1.76805e-07