Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Aphasia	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	0.000634223
L1CAM	[NCBI]	6.52743e-05
LGI1	[NCBI]	3.69159e-05
FOXP2	[NCBI]	2.25542e-05
SNCB	[NCBI]	1.05639e-05
ATP1A2	[NCBI]	9.51137e-06
SKP2	[NCBI]	9.38508e-06
GRN	[NCBI]	8.81996e-06
CDKN1B	[NCBI]	6.73573e-06
MAPT	[NCBI]	6.12357e-06
SNCA	[NCBI]	5.33572e-06
APOE	[NCBI]	3.4483e-06
EGFR	[NCBI]	2.87243e-06

OMIM	Link	Information gain
angiomatosis, diffuse corticomeningeal, of divry and van bogaert	[NCBI]	0.00129156
MRXS12	[NCBI]	0.00129156
LKS	[NCBI]	0.00119103
sneddon syndrome	[NCBI]	0.000817902
FTD	[NCBI]	0.000780702
masa syndrome	[NCBI]	0.000526437
L1CAM	[NCBI]	0.00042158
SPCH1	[NCBI]	0.000221619
HSR	[NCBI]	0.000148925
gliosis, familial progressive subcortical	[NCBI]	7.70698e-05
ADLTE	[NCBI]	6.14197e-05
SLE	[NCBI]	6.0176e-05
LGI1	[NCBI]	5.89764e-05
pick disease of brain	[NCBI]	5.83982e-05
FTLDU	[NCBI]	5.75064e-05
FHM2	[NCBI]	5.75064e-05
PLOSL	[NCBI]	5.66621e-05
MTND5	[NCBI]	5.48274e-05
CADASIL	[NCBI]	4.62276e-05
NF1	[NCBI]	2.75501e-05
CJD	[NCBI]	1.50081e-05
amyloidosis vi	[NCBI]	1.42899e-05
AD	[NCBI]	1.16745e-05
MDD	[NCBI]	7.38034e-06