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01 Abnormalities, Drug-Induced [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.000158514
SHH [NCBI] 3.68214e-05
AHR [NCBI] 3.65167e-05
EGF [NCBI] 2.53304e-05
AR [NCBI] 2.08267e-05
PAX1 [NCBI] 2.06423e-05
ACHE [NCBI] 1.86914e-05
ARSF [NCBI] 1.38369e-05
ARSD [NCBI] 1.38369e-05
KCNH6 [NCBI] 1.23307e-05
PAX6 [NCBI] 1.1869e-05
HOXA3 [NCBI] 1.15758e-05
SMARCD3 [NCBI] 1.12884e-05
FOLR1 [NCBI] 1.071e-05
ARSE [NCBI] 9.79588e-06
HOXA11 [NCBI] 9.58769e-06
WNT7A [NCBI] 8.87625e-06
FGD1 [NCBI] 8.81277e-06
PTGS1 [NCBI] 8.75285e-06
AQP5 [NCBI] 8.47465e-06
G6PD [NCBI] 8.2692e-06
ISL1 [NCBI] 8.14973e-06
WNT4 [NCBI] 7.84125e-06
SMO [NCBI] 7.55016e-06
CAT [NCBI] 7.21084e-06
CBX4 [NCBI] 7.2019e-06
WNT5A [NCBI] 6.87267e-06
INSL3 [NCBI] 6.66633e-06
PAFAH1B1 [NCBI] 6.58026e-06
CYP1A2 [NCBI] 6.17887e-06
NOG [NCBI] 5.9913e-06
GHR [NCBI] 5.89922e-06
MAP2 [NCBI] 5.60238e-06
NAT1 [NCBI] 5.45012e-06
CYP1B1 [NCBI] 5.35045e-06
PAX3 [NCBI] 5.16024e-06
PDGFA [NCBI] 4.7047e-06
PRL [NCBI] 4.69787e-06
NKX2-1 [NCBI] 4.43418e-06
PIH [NCBI] 4.21444e-06
NAT2 [NCBI] 3.94109e-06
CHAT [NCBI] 3.49985e-06
EGFR [NCBI] 3.43797e-06
GSTT1 [NCBI] 3.28267e-06
ADA [NCBI] 3.08279e-06
GSTM1 [NCBI] 2.9792e-06
VIP [NCBI] 2.85199e-06
TH [NCBI] 2.42191e-06
MTHFR [NCBI] 2.34491e-06
NPY [NCBI] 2.07801e-06
AFP [NCBI] 1.46578e-06
PCNA [NCBI] 1.29817e-06
PTH [NCBI] 8.05212e-07



OMIM


 OMIM Link Information
gain		 01
coffin-siris syndrome [NCBI] 0.00113995
CPI [NCBI] 0.000957272
maxillonasal dysplasia, binder type [NCBI] 0.000693453
PCA [NCBI] 0.000607858
isotretinoin embryopathy-like syndrome [NCBI] 0.000555855
chondrodysplasia punctata, autosomal dominant [NCBI] 0.000549018
valproate embryopathy, susceptibility to [NCBI] 0.0005318
poland syndrome [NCBI] 0.000412535
DWS [NCBI] 0.000383542
AOS [NCBI] 0.000383542
OFC1 [NCBI] 0.00034134
SHH [NCBI] 0.000332296
EPHX1 [NCBI] 0.000255518
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 0.000241448
vitamin k-dependent clotting factors, combined deficiency of, 1 [NCBI] 0.000241097
carbimazole sensitivity [NCBI] 0.000194053
AHR [NCBI] 0.000133783
radius, aplasia of, with cleft lip/palate [NCBI] 0.000119344
RA [NCBI] 0.000104032
SLOS [NCBI] 0.000103659
breasts and nipples, absence of [NCBI] 9.6882e-05
CYP26B1 [NCBI] 7.68849e-05
ARSF [NCBI] 7.68849e-05
hypospadias, autosomal [NCBI] 7.05545e-05
por deficiency [NCBI] 6.67384e-05
omphalocele [NCBI] 6.51248e-05
DGS [NCBI] 6.2294e-05
RTD [NCBI] 5.43767e-05
AR [NCBI] 5.12521e-05
epidermolysis bullosa with pyloric atresia [NCBI] 5.02757e-05
CDH2 [NCBI] 5.00331e-05
ABS [NCBI] 4.85676e-05
TGIF [NCBI] 4.83729e-05
SCDO1 [NCBI] 4.70281e-05
ARSE [NCBI] 4.69523e-05
AQP5 [NCBI] 4.69523e-05
RCDP1 [NCBI] 4.51872e-05
RBS [NCBI] 4.47592e-05
POR [NCBI] 4.46082e-05
ACHE [NCBI] 4.45112e-05
EGF [NCBI] 4.26635e-05
DFFB [NCBI] 3.74993e-05
HOS [NCBI] 3.72402e-05
TCOF [NCBI] 3.57685e-05
ALGS1 [NCBI] 3.50839e-05
SLE [NCBI] 2.46528e-05
ABCB1 [NCBI] 2.26526e-05
ABCG2 [NCBI] 2.1739e-05
GHR [NCBI] 1.97522e-05
MAP2 [NCBI] 1.94475e-05
WBS [NCBI] 1.93896e-05
FGFR2 [NCBI] 1.87979e-05
CYP1A1 [NCBI] 1.51596e-05
G6PD [NCBI] 1.47647e-05
TP53 [NCBI] 1.4094e-05
BWS [NCBI] 1.31166e-05
CAT [NCBI] 1.26384e-05
ACE [NCBI] 1.22796e-05
VEGF [NCBI] 1.20418e-05
CHAT [NCBI] 5.57501e-06
FMF [NCBI] 5.1141e-06
ADA [NCBI] 3.8628e-06
VIP [NCBI] 2.90087e-06
PRL [NCBI] 2.29497e-06
PTH [NCBI] 1.71953e-06
TH [NCBI] 1.36761e-06
EGFR [NCBI] 8.26837e-07
NPY [NCBI] 6.24255e-07
thrombocytopenic purpura, autoimmune [NCBI] 4.77213e-07
PCNA [NCBI] 1.21233e-07
AFP [NCBI] 4.11678e-09



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