Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Cerebellar Nuclei	[NCBI]

Gene	Link	Information Gain
SCA20	[NCBI]	0.000510938
MS	[NCBI]	2.57971e-05
CDKL2	[NCBI]	1.71514e-05
ATN1	[NCBI]	1.45176e-05
ALDH5A1	[NCBI]	1.37576e-05
CDH4	[NCBI]	1.26829e-05
RELN	[NCBI]	8.66201e-06
INA	[NCBI]	7.79269e-06
AP1S2	[NCBI]	7.00278e-06
CALB2	[NCBI]	6.69226e-06
CHAT	[NCBI]	5.69197e-06
KLC1	[NCBI]	5.59302e-06
ATXN2	[NCBI]	5.50786e-06
PANK2	[NCBI]	5.45488e-06
ASCL1	[NCBI]	5.34505e-06
CCK	[NCBI]	5.06388e-06
HAPLN1	[NCBI]	4.36654e-06
NGFR	[NCBI]	4.25616e-06
NTN1	[NCBI]	4.05077e-06
HFE	[NCBI]	3.94363e-06
TFRC	[NCBI]	3.74274e-06
MAPT	[NCBI]	3.57017e-06
PAX6	[NCBI]	3.06366e-06
CD68	[NCBI]	2.55668e-06
AVP	[NCBI]	1.97631e-06
GFAP	[NCBI]	1.73003e-06
TH	[NCBI]	1.61298e-06
NPY	[NCBI]	1.51369e-06

OMIM	Link	Information gain
IBGC1	[NCBI]	0.00318854
basal ganglia calcification, idiopathic, childhood-onset	[NCBI]	0.00227639
DRPLA	[NCBI]	0.00192697
nystagmus, voluntary	[NCBI]	0.00154746
opticocochleodentate degeneration	[NCBI]	0.00123667
SCA20	[NCBI]	0.00123667
IOSCA	[NCBI]	0.000942047
MJD	[NCBI]	0.00046523
amyotrophic lateral sclerosis with polyglucosan bodies	[NCBI]	0.00021531
haw river syndrome	[NCBI]	0.000161236
myoclonus and ataxia	[NCBI]	0.000151622
MRX59	[NCBI]	0.000144477
myoclonic epilepsy of unverricht and lundborg	[NCBI]	9.78539e-05
CRH	[NCBI]	9.75596e-05
DRPLA	[NCBI]	8.89991e-05
fabry disease	[NCBI]	6.41014e-05
SMAX1	[NCBI]	5.59427e-05
AP1S2	[NCBI]	4.8888e-05
CACNA1A	[NCBI]	3.42238e-05
TS	[NCBI]	3.13604e-05
ALD	[NCBI]	2.86495e-05
NGFR	[NCBI]	2.32337e-05
CHAT	[NCBI]	2.05101e-05
CCK	[NCBI]	1.63965e-05
AVP	[NCBI]	1.57825e-05
GFAP	[NCBI]	3.37726e-06
TH	[NCBI]	2.74676e-06
NPY	[NCBI]	2.25644e-06
AD	[NCBI]	1.2903e-06