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MeSH keywords -> Related genes, diseases (OMIM)


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01 Death, Sudden [NCBI]

Gene


 Gene Link Information
Gain		 01
GER [NCBI] 0.000158688
SCN5A [NCBI] 5.18757e-05
KCNQ1 [NCBI] 2.1202e-05
CASQ2 [NCBI] 2.04357e-05
MB [NCBI] 1.5496e-05
GPD1L [NCBI] 1.33444e-05
LMNA [NCBI] 1.31815e-05
SCNM1 [NCBI] 1.23272e-05
SOX6 [NCBI] 1.14481e-05
NPR1 [NCBI] 9.99314e-06
ACADVL [NCBI] 9.99314e-06
HADHA [NCBI] 9.72169e-06
ACADM [NCBI] 9.72169e-06
TPH2 [NCBI] 8.93157e-06
NR3C2 [NCBI] 8.73266e-06
TGFB3 [NCBI] 8.31791e-06
ACE2 [NCBI] 8.17663e-06
MYBPC3 [NCBI] 7.89595e-06
TSC1 [NCBI] 7.63025e-06
SCN1A [NCBI] 7.48869e-06
TNNT2 [NCBI] 7.40047e-06
PHOX2B [NCBI] 7.0345e-06
LIPC [NCBI] 6.80778e-06
MYH7 [NCBI] 6.79269e-06
ILK [NCBI] 6.7629e-06
CYP27A1 [NCBI] 6.32344e-06
PTGES2 [NCBI] 5.89391e-06
SMAD2 [NCBI] 5.46821e-06
SMAD3 [NCBI] 5.42106e-06
KCNH6 [NCBI] 5.37521e-06
PRKCB [NCBI] 4.77497e-06
MEN1 [NCBI] 4.6748e-06
MECP2 [NCBI] 4.54884e-06
CDKN2B [NCBI] 4.47245e-06
SMAD4 [NCBI] 4.28256e-06
F2 [NCBI] 4.20484e-06
F5 [NCBI] 3.85678e-06
ESR1 [NCBI] 3.70659e-06
CETP [NCBI] 3.47708e-06
VIP [NCBI] 3.23069e-06
CALCA [NCBI] 3.16261e-06
TLR4 [NCBI] 2.99819e-06
TH [NCBI] 2.79201e-06
NOS3 [NCBI] 2.61471e-06
NPY [NCBI] 2.43905e-06
NOS2 [NCBI] 2.41746e-06
TGFB1 [NCBI] 2.0198e-06
GFAP [NCBI] 1.92941e-06
EPO [NCBI] 1.85772e-06
APOE [NCBI] 1.56637e-06
CASP3 [NCBI] 1.42406e-06
CDKN1A [NCBI] 1.28019e-06
PTH [NCBI] 1.09706e-06
PTGS2 [NCBI] 1.09414e-06



OMIM


 OMIM Link Information
gain		 01
chiari malformation type ii [NCBI] 0.00108068
MVP [NCBI] 0.000996868
splenic hypoplasia [NCBI] 0.000687918
LQT1 [NCBI] 0.000551044
JLNS1 [NCBI] 0.000411762
CMH [NCBI] 0.000374823
proteus syndrome [NCBI] 0.000326916
SPS [NCBI] 0.000317551
hypertelorism with esophageal abnormality and hypospadias [NCBI] 0.000311633
cardiac conduction defect [NCBI] 0.00026978
ARVD1 [NCBI] 0.000216099
apnea, obstructive sleep [NCBI] 0.000196417
VF [NCBI] 0.000182224
brugada syndrome 1 [NCBI] 0.000128313
ACADM [NCBI] 0.000124307
PWS [NCBI] 0.000121681
sudden infant death syndrome [NCBI] 0.000121438
RA [NCBI] 0.000114047
HADHA [NCBI] 0.000110828
sickle cell anemia [NCBI] 9.68791e-05
cardiac arrhythmia [NCBI] 9.57739e-05
crisponi syndrome [NCBI] 8.73026e-05
brugada syndrome 2 [NCBI] 8.73026e-05
SCN5A [NCBI] 8.51818e-05
optic nerve hypoplasia, bilateral [NCBI] 8.18052e-05
carnitine palmitoyltransferase ii deficiency, infantile [NCBI] 8.18052e-05
aortic aneurysm, familial thoracic 4 [NCBI] 8.18052e-05
acyl-coa dehydrogenase, long-chain, deficiency of [NCBI] 7.17636e-05
MB [NCBI] 6.81382e-05
GPD1L [NCBI] 6.55281e-05
NPR1 [NCBI] 6.55281e-05
SOX6 [NCBI] 6.55281e-05
trifunctional protein deficiency [NCBI] 6.25585e-05
CMD3B [NCBI] 6.12169e-05
LGMD1B [NCBI] 6.12169e-05
wolff-parkinson-white syndrome [NCBI] 5.77611e-05
KCNJ8 [NCBI] 5.76429e-05
acyl-coa dehydrogenase, very long-chain, deficiency of [NCBI] 5.67583e-05
CRLF1 [NCBI] 5.59803e-05
septooptic dysplasia [NCBI] 5.58151e-05
EDMD2 [NCBI] 5.25211e-05
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency [NCBI] 5.17949e-05
CPT2 [NCBI] 4.94846e-05
ACADVL [NCBI] 4.87212e-05
andersen cardiodysrhythmic periodic paralysis [NCBI] 4.8028e-05
3-@hydroxy-3-methylglutaryl-coa lyase deficiency [NCBI] 4.45812e-05
RYR2 [NCBI] 4.16745e-05
MYH11 [NCBI] 4.16745e-05
oca2 gene [NCBI] 4.13214e-05
EDMD [NCBI] 3.86876e-05
aortic valve disease [NCBI] 3.66981e-05
MYH7 [NCBI] 3.5485e-05
CF [NCBI] 3.21879e-05
SVAS [NCBI] 3.13879e-05
MTTL1 [NCBI] 3.11023e-05
GNAS [NCBI] 3.09816e-05
ILK [NCBI] 2.88397e-05
ADCYAP1 [NCBI] 2.62519e-05
WBS [NCBI] 1.84252e-05
NF1 [NCBI] 1.77014e-05
dystrophia myotonica 1 [NCBI] 1.6118e-05
RTT [NCBI] 1.52234e-05
MUC1 [NCBI] 1.02784e-05
VIP [NCBI] 8.30424e-06
temporal arteritis [NCBI] 7.56235e-06
TH [NCBI] 5.99391e-06
NPY [NCBI] 4.59418e-06
GFAP [NCBI] 2.53489e-06
EPO [NCBI] 2.31752e-06
PTH [NCBI] 2.46085e-07
MG [NCBI] 3.21912e-08



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