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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



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