MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Asphyxia Neonatorum
[NCBI]
Gene
Gene
Link
Information
Gain
01
GER
[NCBI]
0.000158688
EPO
[NCBI]
2.99417e-05
TH
[NCBI]
2.11883e-05
CASP3
[NCBI]
2.0792e-05
GFAP
[NCBI]
1.74183e-05
GHRH
[NCBI]
1.67664e-05
AVP
[NCBI]
1.41456e-05
ALB
[NCBI]
1.2025e-05
PIH
[NCBI]
1.19331e-05
SLC1A1
[NCBI]
9.45303e-06
SDC2
[NCBI]
8.90416e-06
SLC18A3
[NCBI]
8.90416e-06
BDNF
[NCBI]
8.34134e-06
CD68
[NCBI]
7.81111e-06
HMGB1
[NCBI]
7.42729e-06
MBP
[NCBI]
7.35687e-06
ADCYAP1
[NCBI]
6.62396e-06
PRL
[NCBI]
5.76126e-06
ADM
[NCBI]
5.6932e-06
IGFBP3
[NCBI]
5.47471e-06
AMBP
[NCBI]
5.33778e-06
HMOX1
[NCBI]
4.61745e-06
IGF1
[NCBI]
4.60276e-06
TTR
[NCBI]
4.3587e-06
CCL2
[NCBI]
3.80084e-06
IL1B
[NCBI]
3.73988e-06
TRH
[NCBI]
3.27292e-06
ACHE
[NCBI]
2.91081e-06
IL6
[NCBI]
2.8923e-06
HIF1A
[NCBI]
2.53616e-06
AKT1
[NCBI]
2.48161e-06
TNF
[NCBI]
2.35708e-06
NGF
[NCBI]
2.00279e-06
AFP
[NCBI]
1.9507e-06
EGF
[NCBI]
1.11506e-06
OMIM
OMIM
Link
Information
gain
01
ATD1
[NCBI]
0.00990745
cerebral palsy, ataxic, autosomal recessive
[NCBI]
0.000632907
short rib-polydactyly syndrome, type iii
[NCBI]
0.000500764
cerebral palsy, spastic, symmetric, autosomal recessive
[NCBI]
0.000379076
diaphragmatic hernia, congenital
[NCBI]
0.000376956
thoracopelvic dysostosis
[NCBI]
0.000131943
TLPD
[NCBI]
0.000117955
EPO
[NCBI]
9.69967e-05
DSMA1
[NCBI]
9.48731e-05
CDPX2
[NCBI]
7.99294e-05
MTM1
[NCBI]
7.31565e-05
TH
[NCBI]
6.95302e-05
CKB
[NCBI]
6.11901e-05
SLC1A1
[NCBI]
5.12477e-05
GFAP
[NCBI]
5.0301e-05
ALB
[NCBI]
4.43586e-05
SLC18A3
[NCBI]
3.84781e-05
AVP
[NCBI]
3.5473e-05
NPPA
[NCBI]
2.85187e-05
HMBS
[NCBI]
2.59178e-05
BDNF
[NCBI]
2.37843e-05
ADM
[NCBI]
2.35922e-05
MBP
[NCBI]
1.82383e-05
TTR
[NCBI]
1.16152e-05
PRL
[NCBI]
9.96303e-06
ACHE
[NCBI]
5.26212e-06
NGFB
[NCBI]
1.74147e-06
AFP
[NCBI]
1.66914e-06
TNF
[NCBI]
1.17656e-06
EGF
[NCBI]
4.27955e-09
Database Center for Life Science