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01 Autonomic Nervous System Diseases [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.00110048
PKC [NCBI] 0.00011198
ACHE [NCBI] 5.46102e-05
TTR [NCBI] 5.25963e-05
PHOX2B [NCBI] 4.32258e-05
CHAT [NCBI] 3.45095e-05
DBH [NCBI] 3.04233e-05
SNCA [NCBI] 2.41797e-05
EPO [NCBI] 2.15816e-05
NGF [NCBI] 2.15603e-05
VAPB [NCBI] 2.02629e-05
AAAS [NCBI] 1.64947e-05
SLC18A2 [NCBI] 1.5967e-05
AVP [NCBI] 1.53589e-05
SLC6A2 [NCBI] 1.38185e-05
PARK2 [NCBI] 1.37789e-05
KCNA6 [NCBI] 1.21299e-05
GFRA3 [NCBI] 1.07675e-05
TH [NCBI] 1.03111e-05
KCNA2 [NCBI] 9.82824e-06
ARTN [NCBI] 9.65646e-06
LEP [NCBI] 9.14904e-06
ECE1 [NCBI] 8.59495e-06
GRK1 [NCBI] 8.50927e-06
GCLC [NCBI] 8.27536e-06
CHRNB4 [NCBI] 8.27536e-06
TCF4 [NCBI] 8.06967e-06
NTRK2 [NCBI] 7.88614e-06
CHRNA3 [NCBI] 7.82911e-06
GAST [NCBI] 7.5695e-06
S100P [NCBI] 7.38701e-06
KCNA1 [NCBI] 7.3443e-06
CSRP3 [NCBI] 7.07204e-06
RAB7A [NCBI] 6.80648e-06
TLX1 [NCBI] 6.71673e-06
SNAP25 [NCBI] 6.52416e-06
SDHB [NCBI] 6.1316e-06
CCK [NCBI] 6.0262e-06
SDHD [NCBI] 6.01235e-06
TGM1 [NCBI] 5.69832e-06
BDNF [NCBI] 5.69247e-06
MPZ [NCBI] 5.57568e-06
NPPA [NCBI] 5.51759e-06
NGFR [NCBI] 5.1943e-06
SPN [NCBI] 4.97458e-06
PTH [NCBI] 4.93277e-06
LRRK2 [NCBI] 4.63229e-06
CACNA1A [NCBI] 4.29434e-06
NEFH [NCBI] 4.13938e-06
CD99 [NCBI] 3.95914e-06
HLA-A [NCBI] 3.60152e-06
PIH [NCBI] 3.43943e-06
MECP2 [NCBI] 3.38135e-06
HLA-B [NCBI] 3.20903e-06
APOE [NCBI] 3.10636e-06
COMT [NCBI] 2.90849e-06
SLC6A4 [NCBI] 2.67296e-06
HLA-DQB1 [NCBI] 2.46238e-06
CST3 [NCBI] 2.37355e-06
FMR1 [NCBI] 2.36023e-06
VIP [NCBI] 2.12109e-06
HLA-DRB1 [NCBI] 1.90494e-06
SOD1 [NCBI] 1.87964e-06
NPY [NCBI] 1.39755e-06
NOS2 [NCBI] 1.37839e-06
PRL [NCBI] 7.34266e-07
EGF [NCBI] 2.52594e-07



OMIM


 OMIM Link Information
gain		 01
megacystis-microcolon-intestinal hypoperistalsis syndrome [NCBI] 0.00140547
indifference to pain, congenital, autosomal dominant [NCBI] 0.000787083
apnea, obstructive sleep [NCBI] 0.000348113
EKD1 [NCBI] 0.000332391
HSAN3 [NCBI] 0.000315972
autonomic control, congenital failure of [NCBI] 0.00026481
dopamine beta-hydroxylase deficiency, congenital [NCBI] 0.000245654
ACHE [NCBI] 0.000185777
FFI [NCBI] 0.000183321
CVS [NCBI] 0.000174917
HSCR1 [NCBI] 0.000168615
hypotension, orthostatic [NCBI] 0.000161685
TTR [NCBI] 0.000157891
lipomatosis, familial benign cervical [NCBI] 0.000141995
CHAT [NCBI] 0.000121262
GIST [NCBI] 0.000116233
motor neuropathy, peripheral, with dysautonomia [NCBI] 0.000114645
neuropathy, hereditary sensory, x-linked [NCBI] 0.000114645
DBH [NCBI] 9.94703e-05
PD [NCBI] 8.94791e-05
neuronal intranuclear inclusion disease [NCBI] 8.37176e-05
porphyria variegata [NCBI] 8.05786e-05
PTHS [NCBI] 7.41406e-05
HSAN5 [NCBI] 7.08902e-05
aromatic l-amino acid decarboxylase deficiency [NCBI] 7.08902e-05
fabry disease [NCBI] 6.64654e-05
PARK4 [NCBI] 6.38614e-05
GCLC [NCBI] 6.17915e-05
PARK1 [NCBI] 5.76592e-05
VAV3 [NCBI] 5.6595e-05
indifference to pain, congenital, autosomal recessive [NCBI] 5.64247e-05
EPO [NCBI] 5.26051e-05
NGFB [NCBI] 5.17865e-05
NHLH1 [NCBI] 5.07153e-05
TCF4 [NCBI] 4.87186e-05
AAA [NCBI] 4.75732e-05
AVP [NCBI] 4.66466e-05
ECE1 [NCBI] 4.56389e-05
MJD [NCBI] 4.27713e-05
IKBKAP [NCBI] 4.23054e-05
NTRK2 [NCBI] 3.78397e-05
PHOX2B [NCBI] 3.67119e-05
coproporphyria [NCBI] 2.95242e-05
GPT [NCBI] 2.63274e-05
SNCA [NCBI] 2.35332e-05
FRDA [NCBI] 2.28926e-05
NGFR [NCBI] 2.28859e-05
TH [NCBI] 2.28609e-05
MPZ [NCBI] 2.14967e-05
SLE [NCBI] 2.09512e-05
FMF [NCBI] 1.91676e-05
RET [NCBI] 1.82816e-05
NPPA [NCBI] 1.47908e-05
RTT [NCBI] 1.23174e-05
CCK [NCBI] 1.14667e-05
BDNF [NCBI] 1.07934e-05
NF1 [NCBI] 9.721e-06
COMT [NCBI] 8.63443e-06
RA [NCBI] 7.66527e-06
ALD [NCBI] 6.12978e-06
GDNF [NCBI] 6.07617e-06
AD [NCBI] 5.3954e-06
APOE [NCBI] 4.09833e-06
EGF [NCBI] 3.90984e-06
MDD [NCBI] 3.60998e-06
PTH [NCBI] 2.55442e-06
VIP [NCBI] 2.17045e-06
CD [NCBI] 2.11663e-06
MG [NCBI] 7.2e-07
PRL [NCBI] 5.36949e-07
CRH [NCBI] 4.59702e-07
NPY [NCBI] 2.73338e-07



Database Center for Life Science