Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Epilepsy, Complex Partial	[NCBI]

Gene	Link	Information Gain
BAFME2	[NCBI]	0.000415947
MS	[NCBI]	3.75925e-05
SLC4A10	[NCBI]	1.65752e-05
SCN3A	[NCBI]	1.43136e-05
SCO1	[NCBI]	1.29021e-05
DCX	[NCBI]	1.18181e-05
SGCE	[NCBI]	1.09707e-05
FLNA	[NCBI]	1.06467e-05
AIF1	[NCBI]	1.05745e-05
SCN1A	[NCBI]	9.81521e-06
PAFAH1B1	[NCBI]	9.30774e-06
CP	[NCBI]	7.80187e-06
CACNA1A	[NCBI]	7.79489e-06
TTR	[NCBI]	6.48256e-06
NPY	[NCBI]	4.64652e-06
GFAP	[NCBI]	4.08695e-06
PRL	[NCBI]	3.77837e-06
APOE	[NCBI]	3.67409e-06

OMIM	Link	Information gain
ETL2	[NCBI]	0.00158697
heterotopia, periventricular, associated with chromosome 5p anomalies	[NCBI]	0.00119841
epilepsy, myoclonic, benign adult familial, type 2	[NCBI]	0.00098052
alopecia, psychomotor epilepsy, pyorrhea, and mental subnormality	[NCBI]	0.00098052
amyloidosis vii	[NCBI]	0.000100104
heterotopia, periventricular, x-linked dominant	[NCBI]	9.27799e-05
SCA10	[NCBI]	8.92647e-05
myoclonic dystonia	[NCBI]	7.99294e-05
SGCE	[NCBI]	5.63183e-05
FLNA	[NCBI]	5.00962e-05
CACNA1A	[NCBI]	4.72778e-05
GTS	[NCBI]	4.11849e-05
TS	[NCBI]	3.70827e-05
CP	[NCBI]	3.2154e-05
CJD	[NCBI]	2.58282e-05
TTR	[NCBI]	2.29303e-05
NPY	[NCBI]	1.37146e-05
APOE	[NCBI]	1.17302e-05
GFAP	[NCBI]	1.08059e-05
PRL	[NCBI]	8.94895e-06
VEGF	[NCBI]	1.76921e-06