Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Olivopontocerebellar Atrophies	[NCBI]

Gene	Link	Information Gain
ITPR1	[NCBI]	3.09082e-05
RABEP1	[NCBI]	1.40278e-05
SLC1A6	[NCBI]	1.36821e-05
SNCA	[NCBI]	1.23333e-05
SLC1A1	[NCBI]	1.09805e-05
GNAI2	[NCBI]	1.08556e-05
SLC1A2	[NCBI]	1.03847e-05
SLC1A3	[NCBI]	1.03395e-05
SLC18A2	[NCBI]	9.68155e-06
GFAP	[NCBI]	9.34638e-06
ATXN2	[NCBI]	8.19521e-06
NEFL	[NCBI]	7.65438e-06
ATXN1	[NCBI]	7.61771e-06
CDK5	[NCBI]	7.50369e-06
PARK2	[NCBI]	5.58316e-06
CHAT	[NCBI]	5.54551e-06
VHL	[NCBI]	5.37145e-06
FMR1	[NCBI]	5.13106e-06
TRH	[NCBI]	4.74326e-06
TH	[NCBI]	4.40841e-06
MBP	[NCBI]	3.9852e-06
BAX	[NCBI]	3.53444e-06
FASLG	[NCBI]	3.43314e-06
CASP3	[NCBI]	2.91434e-06

OMIM	Link	Information gain
cerebellar atrophy with progressive microcephaly	[NCBI]	0.00236517
pontocerebellar hypoplasia, type 1	[NCBI]	0.00107364
pontocerebellar hypoplasia, type 2	[NCBI]	0.000991404
SCAX1	[NCBI]	0.000840405
MJD	[NCBI]	0.000434922
CDG1A	[NCBI]	0.000317221
encephalopathy, fatal infantile, with olivopontocerebellar hypoplasia	[NCBI]	0.000269279
SCA2	[NCBI]	0.000118376
SCA1	[NCBI]	0.000110727
branchial myoclonus with spastic paraparesis and cerebellar ataxia	[NCBI]	9.3728e-05
DSMA1	[NCBI]	7.47703e-05
FXTAS	[NCBI]	7.2683e-05
SCA6	[NCBI]	5.60054e-05
SCA7	[NCBI]	5.28878e-05
GFAP	[NCBI]	4.26686e-05
DRPLA	[NCBI]	3.70749e-05
CHAT	[NCBI]	2.57724e-05
HD	[NCBI]	2.54263e-05
TH	[NCBI]	1.90138e-05
CRH	[NCBI]	1.78773e-05
MBP	[NCBI]	1.70458e-05
CJD	[NCBI]	8.9227e-06