Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Nerve Compression Syndromes	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	0.000105673
PMP22	[NCBI]	9.79977e-05
NEFH	[NCBI]	2.473e-05
SOST	[NCBI]	2.29147e-05
NPY	[NCBI]	1.57157e-05
NGF	[NCBI]	1.37658e-05
CACNA1I	[NCBI]	1.37507e-05
LIMS1	[NCBI]	1.09822e-05
ATF3	[NCBI]	8.8264e-06
GFAP	[NCBI]	7.93808e-06
MPZ	[NCBI]	7.76224e-06
ILK	[NCBI]	7.74737e-06
ATP7A	[NCBI]	7.19572e-06
CCK	[NCBI]	3.9667e-06
PTGS2	[NCBI]	1.89619e-06

OMIM	Link	Information gain
CMDR	[NCBI]	0.00092257
CTS1	[NCBI]	0.000766909
HNPP	[NCBI]	0.000595703
superior transverse scapular ligament, calcification of, familial	[NCBI]	0.00026386
SOST	[NCBI]	0.000259777
PMP22	[NCBI]	0.000174705
hyperostosis cranialis interna	[NCBI]	0.000131618
CMT1A	[NCBI]	0.000117416
hemifacial spasm, familial	[NCBI]	0.000100673
ACH	[NCBI]	9.92378e-05
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus	[NCBI]	7.89629e-05
CMDD	[NCBI]	6.65411e-05
NPY	[NCBI]	5.61987e-05
ATF3	[NCBI]	4.58182e-05
NGFB	[NCBI]	4.54063e-05
fabry disease	[NCBI]	3.85627e-05
MAS	[NCBI]	3.83009e-05
ILK	[NCBI]	3.39485e-05
ADCYAP1	[NCBI]	3.13352e-05
MAG	[NCBI]	2.7105e-05
GFAP	[NCBI]	2.35292e-05
CCK	[NCBI]	1.15182e-05
RA	[NCBI]	1.20416e-06
VEGF	[NCBI]	1.2688e-08