Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Oculomotor Nerve	[NCBI]

Gene	Link	Information Gain
NYS2	[NCBI]	0.000336348
MS	[NCBI]	0.000228906
CHAT	[NCBI]	2.52607e-05
PHOX2A	[NCBI]	1.39844e-05
UCN	[NCBI]	1.14562e-05
ISL1	[NCBI]	1.07932e-05
CHN1	[NCBI]	7.3181e-06
KIF21A	[NCBI]	6.87817e-06
PHOX2B	[NCBI]	5.26801e-06
GFAP	[NCBI]	5.17889e-06
ACHE	[NCBI]	5.10516e-06
TH	[NCBI]	4.93354e-06
BCHE	[NCBI]	4.69084e-06
KRT7	[NCBI]	4.49291e-06
NTN1	[NCBI]	4.23566e-06
GRM5	[NCBI]	3.71089e-06
TRH	[NCBI]	2.45199e-06
BDNF	[NCBI]	2.06946e-06
CCK	[NCBI]	2.02733e-06

OMIM	Link	Information gain
PTOS1	[NCBI]	0.00125871
NYS2	[NCBI]	0.00112601
CFEOM3	[NCBI]	0.00101143
MBS	[NCBI]	0.000766398
CFEOM1	[NCBI]	0.00052713
fibrosis of extraocular muscles, congenital, with synergistic divergence	[NCBI]	0.000189204
CFEOM2	[NCBI]	0.000189204
MJD	[NCBI]	0.000187987
adie pupil	[NCBI]	0.000179582
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive	[NCBI]	0.000148404
amyloidosis vii	[NCBI]	0.000148404
CHAT	[NCBI]	0.000117086
KSS	[NCBI]	8.2718e-05
UCN	[NCBI]	6.20103e-05
GDNF	[NCBI]	3.29977e-05
BCHE	[NCBI]	2.28669e-05
TTR	[NCBI]	1.80863e-05
GAL	[NCBI]	1.68739e-05
GFAP	[NCBI]	1.62587e-05
ACHE	[NCBI]	1.58126e-05
TH	[NCBI]	1.4633e-05
BDNF	[NCBI]	4.96098e-06
CCK	[NCBI]	4.63938e-06