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MeSH keywords -> Related genes, diseases (OMIM)


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01 Sleep Stages [NCBI]


Gene


Gene Link Information
Gain
01
MS [NCBI] 8.6708e-05
GTS [NCBI] 8.62108e-05
GER [NCBI] 4.60628e-05
PRL [NCBI] 4.48318e-05
GHRH [NCBI] 7.7961e-06
TNF [NCBI] 7.07899e-06
CRH [NCBI] 6.59687e-06
PTGDS [NCBI] 5.84687e-06
ACHE [NCBI] 5.15661e-06
PHOX2B [NCBI] 4.61903e-06
TRH [NCBI] 4.20938e-06
GHRL [NCBI] 4.04659e-06
PRNP [NCBI] 3.71904e-06
AVP [NCBI] 3.60838e-06
CCK [NCBI] 3.59886e-06
IER5 [NCBI] 3.4654e-06
INMT [NCBI] 3.40018e-06
NPY [NCBI] 3.24318e-06
POMC [NCBI] 3.17025e-06
PGDS [NCBI] 3.13257e-06
HCRT [NCBI] 2.77699e-06
IL1RN [NCBI] 2.56389e-06
ACADM [NCBI] 2.53262e-06
PER3 [NCBI] 2.48161e-06
GABBR1 [NCBI] 2.45811e-06
PER2 [NCBI] 2.12662e-06
ATXN2 [NCBI] 2.03699e-06
TH [NCBI] 2.03416e-06
PINK1 [NCBI] 2.01353e-06
ATXN3 [NCBI] 1.83051e-06
IL18 [NCBI] 1.77005e-06
CYP1A2 [NCBI] 1.72274e-06
CHGA [NCBI] 1.7168e-06
DBH [NCBI] 1.64973e-06
GDNF [NCBI] 1.55711e-06
ALDH2 [NCBI] 1.54489e-06
LEP [NCBI] 1.46348e-06
SERPINE1 [NCBI] 1.34355e-06
ABCB1 [NCBI] 1.24849e-06
HLA-DQB1 [NCBI] 1.23688e-06
COMT [NCBI] 1.17314e-06
SOD1 [NCBI] 1.07566e-06
CHAT [NCBI] 1.01618e-06
SLC6A4 [NCBI] 9.97901e-07
IL6 [NCBI] 9.90026e-07
VIP [NCBI] 7.72972e-07
VWF [NCBI] 7.40008e-07
APOE [NCBI] 6.66753e-07
PTH [NCBI] 5.47121e-07
NGF [NCBI] 4.7194e-07




OMIM


OMIM Link Information
gain
01
apnea, obstructive sleep [NCBI] 0.0319972
MDD [NCBI] 0.000745469
GHRH [NCBI] 0.000307294
centralopathic epilepsy [NCBI] 0.000262842
PRL [NCBI] 0.000240991
ETL2 [NCBI] 0.000230401
CRH [NCBI] 0.000147128
faciomandibular myoclonus, nocturnal [NCBI] 0.000142218
glaucoma and sleep apnea [NCBI] 0.000142218
LKS [NCBI] 0.000126301
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 0.000108095
advanced sleep-phase syndrome, familial [NCBI] 0.000103994
paroxysmal tonic upgaze, benign childhood, with ataxia [NCBI] 9.72023e-05
acyl-coa dehydrogenase, long-chain, deficiency of [NCBI] 9.72023e-05
FFI [NCBI] 9.27653e-05
corpus callosum, agenesis of [NCBI] 7.52459e-05
HCRT [NCBI] 7.39101e-05
SLE [NCBI] 6.94346e-05
sudden infant death syndrome [NCBI] 6.01679e-05
acyl-coa dehydrogenase, medium-chain, deficiency of [NCBI] 5.9313e-05
PWS [NCBI] 5.53029e-05
CVS [NCBI] 5.29641e-05
DM2 [NCBI] 4.73039e-05
PD [NCBI] 4.69188e-05
SCA2 [NCBI] 3.78079e-05
SMS [NCBI] 2.98933e-05
PTGDS [NCBI] 2.6707e-05
PMD [NCBI] 2.63177e-05
NPAS2 [NCBI] 2.57568e-05
GABRB3 [NCBI] 2.45688e-05
RA [NCBI] 2.22976e-05
PMCH [NCBI] 2.21646e-05
PRLH [NCBI] 1.63822e-05
RTT [NCBI] 1.62199e-05
POMC [NCBI] 1.33216e-05
GTS [NCBI] 1.22745e-05
AS [NCBI] 1.18064e-05
AVP [NCBI] 1.16099e-05
IL6 [NCBI] 1.1376e-05
ACHE [NCBI] 1.11367e-05
MG [NCBI] 1.07081e-05
TNF [NCBI] 9.39237e-06
VEGF [NCBI] 6.95699e-06
CCK [NCBI] 6.85781e-06
NPY [NCBI] 3.24658e-06
GDNF [NCBI] 2.3842e-06
NGFB [NCBI] 1.87695e-06
CJD [NCBI] 1.37519e-06
TH [NCBI] 1.13003e-06
PTH [NCBI] 9.59787e-07
CHAT [NCBI] 5.5123e-07
CF [NCBI] 2.14666e-07
APOE [NCBI] 6.57348e-08
VIP [NCBI] 2.15884e-11




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