MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
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
Database Center for Life Science