Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Vestibulocochlear Nerve [NCBI]


Gene


Gene Link Information
Gain
01
MS [NCBI] 0.000383812
HFM [NCBI] 0.00019866
NGF [NCBI] 2.27887e-05
ACHE [NCBI] 1.26155e-05
CHAT [NCBI] 1.00027e-05
PRPH [NCBI] 6.85573e-06
KRIT1 [NCBI] 6.03602e-06
MBP [NCBI] 5.83211e-06
BDNF [NCBI] 5.28915e-06
GFAP [NCBI] 4.95002e-06
ISL1 [NCBI] 4.56568e-06
NGFR [NCBI] 4.32611e-06
NEFL [NCBI] 4.16568e-06
MAP2 [NCBI] 3.92188e-06
MARCKS [NCBI] 3.77407e-06
NEFH [NCBI] 3.69743e-06
GRM5 [NCBI] 3.59632e-06
CNTF [NCBI] 3.26554e-06
G6PD [NCBI] 3.21048e-06
PCNA [NCBI] 2.01413e-06




OMIM


OMIM Link Information
gain
01
auditory neuropathy, x-linked, 1, with peripheral sensory neuropathy [NCBI] 0.00145218
auditory neuropathy, autosomal dominant, 1 [NCBI] 0.00145218
HFM [NCBI] 0.000761113
NF2 [NCBI] 0.000617688
optic atrophy, hearing loss, and peripheral neuropathy, autosomal recessive [NCBI] 0.000194064
valproate embryopathy, susceptibility to [NCBI] 0.000162475
deafness, aminoglycoside-induced [NCBI] 0.000156777
DFNB9 [NCBI] 0.00015204
hypoparathyroidism, sensorineural deafness, and renal disease [NCBI] 0.000144442
usher syndrome, type i [NCBI] 0.000124035
CSA [NCBI] 0.000104924
CMT1B [NCBI] 0.000101125
fabry disease [NCBI] 8.15972e-05
NGFB [NCBI] 7.25529e-05
OTOF [NCBI] 3.98141e-05
ACHE [NCBI] 3.89151e-05
CHAT [NCBI] 3.26756e-05
GDNF [NCBI] 2.68775e-05
NGFR [NCBI] 2.09625e-05
MAP2 [NCBI] 1.69029e-05
MBP [NCBI] 1.65442e-05
BDNF [NCBI] 1.31097e-05
GFAP [NCBI] 1.09305e-05
CNTF [NCBI] 1.04645e-05
SPP1 [NCBI] 9.49258e-06
G6PD [NCBI] 9.18769e-06
PCNA [NCBI] 3.06311e-06
CF [NCBI] 1.53266e-08




Database Center for Life Science