Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Cranial Nerve Diseases	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	0.000206848
HFM	[NCBI]	0.000166043
NGF	[NCBI]	2.61795e-05
PMP22	[NCBI]	1.6272e-05
KCNA6	[NCBI]	1.56767e-05
PXMP2	[NCBI]	1.35648e-05
KCNA2	[NCBI]	1.33737e-05
TBCE	[NCBI]	1.22289e-05
KCNA1	[NCBI]	1.08838e-05
EGR2	[NCBI]	1.07612e-05
CD99	[NCBI]	7.44922e-06
NOD2	[NCBI]	6.0236e-06
ADA	[NCBI]	5.73202e-06
PRL	[NCBI]	3.77837e-06

OMIM	Link	Information gain
MBS	[NCBI]	0.00584596
amyloidosis v	[NCBI]	0.000390306
HFM	[NCBI]	0.000282209
SOST	[NCBI]	0.000165458
fourth cranial nerve palsy, familial congenital	[NCBI]	0.000135008
hyperostosis cranialis interna	[NCBI]	0.000135008
osteopetrosis and infantile neuroaxonal dystrophy	[NCBI]	0.000104061
OPTB2	[NCBI]	9.44644e-05
NGFB	[NCBI]	9.43078e-05
cerebellotrigeminal dermal dysplasia	[NCBI]	9.12041e-05
sc phocomelia syndrome	[NCBI]	8.07248e-05
wildervanck syndrome	[NCBI]	7.92529e-05
synovitis, granulomatous, with uveitis and cranial neuropathies	[NCBI]	7.34171e-05
ESCO2	[NCBI]	6.99095e-05
TBCE	[NCBI]	6.62447e-05
ODDD	[NCBI]	6.10678e-05
RBS	[NCBI]	6.01869e-05
TBX1	[NCBI]	5.69829e-05
EGR2	[NCBI]	5.58467e-05
LSA	[NCBI]	5.05385e-05
DGS	[NCBI]	3.51753e-05
MG	[NCBI]	2.83496e-05
temporal arteritis	[NCBI]	2.10286e-05
ADA	[NCBI]	1.88033e-05
PRL	[NCBI]	8.1404e-06
KLK3	[NCBI]	5.00333e-06
SLE	[NCBI]	4.21892e-07