Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Apnea [NCBI]

Gene


 Gene Link Information
Gain		 01
GER [NCBI] 0.00430176
BCHE [NCBI] 4.12908e-05
PHOX2B [NCBI] 3.09331e-05
CHAT [NCBI] 2.13003e-05
SLC9A3 [NCBI] 1.74379e-05
ADK [NCBI] 1.23502e-05
AHI1 [NCBI] 1.09476e-05
UGT2B7 [NCBI] 1.08696e-05
PTGER3 [NCBI] 1.05888e-05
TCF4 [NCBI] 1.05888e-05
SLC5A3 [NCBI] 1.05252e-05
AVP [NCBI] 1.02897e-05
CBX4 [NCBI] 8.91064e-06
MB [NCBI] 7.84314e-06
CYP2D6 [NCBI] 7.20957e-06
F2 [NCBI] 5.4836e-06
F5 [NCBI] 5.1285e-06
TRH [NCBI] 4.3617e-06
CAT [NCBI] 4.09536e-06
ACHE [NCBI] 3.9874e-06
MTHFR [NCBI] 3.94668e-06



OMIM


 OMIM Link Information
gain		 01
apnea, obstructive sleep [NCBI] 0.00146507
fatty metamorphosis of viscera [NCBI] 0.00138193
JBTS1 [NCBI] 0.000971903
JBTS2 [NCBI] 0.000613493
breath-holding spells [NCBI] 0.000611213
mohr syndrome [NCBI] 0.000473781
varadi-papp syndrome [NCBI] 0.000462747
BCHE [NCBI] 0.000428876
myasthenic syndrome, congenital, associated with episodic apnea [NCBI] 0.00027669
sudden infant death syndrome [NCBI] 0.000153803
dandy-walker malformation with postaxial polydactyly [NCBI] 0.000111802
ACH [NCBI] 0.00010457
JBTS5 [NCBI] 0.000103324
SLC5A3 [NCBI] 8.76514e-05
JBTS3 [NCBI] 8.54378e-05
corpus callosum, agenesis of [NCBI] 8.34102e-05
CHAT [NCBI] 7.59109e-05
MUSK [NCBI] 7.38721e-05
septooptic dysplasia [NCBI] 7.17329e-05
myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency [NCBI] 6.63054e-05
TLX3 [NCBI] 6.27854e-05
autonomic control, congenital failure of [NCBI] 6.22591e-05
AHI1 [NCBI] 5.76986e-05
ADK [NCBI] 5.76986e-05
hurler syndrome [NCBI] 5.05277e-05
AVP [NCBI] 4.69751e-05
MB [NCBI] 3.01703e-05
RTT [NCBI] 2.95253e-05
ADCYAP1 [NCBI] 2.93246e-05
PWS [NCBI] 1.50375e-05
SLE [NCBI] 1.33498e-05
PD [NCBI] 1.21748e-05
CAT [NCBI] 9.32432e-06
ACHE [NCBI] 8.39656e-06



Database Center for Life Science