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MeSH keywords -> Related genes, diseases (OMIM)


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01 Cranial Nerve Diseases [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science