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01 Ductus Arteriosus, Patent [NCBI]

Gene


 Gene Link Information
Gain		 01
GER [NCBI] 0.000158688
TFAP2B [NCBI] 6.88874e-05
MYH11 [NCBI] 3.99301e-05
NKX2-5 [NCBI] 1.98009e-05
KCNB1 [NCBI] 1.35962e-05
HOXA3 [NCBI] 1.35962e-05
CRELD1 [NCBI] 1.28474e-05
EVC [NCBI] 1.18154e-05
KCNA5 [NCBI] 1.11009e-05
LAMB1 [NCBI] 1.08311e-05
HOXA13 [NCBI] 1.0442e-05
MPO [NCBI] 8.95449e-06
IL12A [NCBI] 8.67818e-06
NPPA [NCBI] 8.32642e-06
LCN2 [NCBI] 7.59689e-06
PTGES2 [NCBI] 7.4963e-06
JAG1 [NCBI] 7.46987e-06
AGTR1 [NCBI] 6.59977e-06
PTPN11 [NCBI] 6.51802e-06
IFNG [NCBI] 6.06196e-06
IGF1 [NCBI] 6.02062e-06
AGT [NCBI] 5.65811e-06
NOS3 [NCBI] 4.13802e-06
VEGFA [NCBI] 3.2118e-06



OMIM


 OMIM Link Information
gain		 01
patent ductus arteriosus [NCBI] 0.00315196
char syndrome [NCBI] 0.000951846
splenic hypoplasia [NCBI] 0.00074746
corpus callosum, agenesis of, with facial anomalies and robin sequence [NCBI] 0.000689681
visceral neuropathy, familial, autosomal recessive [NCBI] 0.000647644
aortic aneurysm, familial thoracic 4 [NCBI] 0.000512284
AOS [NCBI] 0.000405392
TFAP2B [NCBI] 0.000367907
MYH11 [NCBI] 0.000312666
intestinal pseudoobstruction, neuronal, chronic idiopathic, x-linked [NCBI] 0.000297703
patent ductus arteriosus and bicuspid aortic valve with hand anomalies [NCBI] 0.000127341
bowen syndrome of multiple malformations [NCBI] 0.000127341
intestinal pseudoobstruction with patent ductus arteriosus and natal teeth [NCBI] 0.000127341
distichiasis with congenital anomalies of the heart and peripheral vasculature [NCBI] 0.000127341
corneal hypesthesia with retinal abnormalities, sensorineural deafness, unusual facies, persistent ductus arteriosus, and mental retardation [NCBI] 0.000127341
aortic arch interruption, facial palsy, and retinal coloboma [NCBI] 0.000104875
stratton-parker syndrome [NCBI] 0.000104875
pulmonic stenosis [NCBI] 8.68069e-05
right ventricular hypoplasia, isolated [NCBI] 8.68069e-05
weyers acrofacial dysostosis [NCBI] 8.3549e-05
bowing of legs, anterior, with dwarfism [NCBI] 8.3549e-05
emanuel syndrome [NCBI] 7.64978e-05
PDV [NCBI] 7.30815e-05
HTX1 [NCBI] 7.1612e-05
PTGER4 [NCBI] 6.86721e-05
alpha-thalassemia/mental retardation syndrome, deletion-type [NCBI] 6.67957e-05
NPPA [NCBI] 6.65398e-05
KFSD [NCBI] 6.39453e-05
asplenia with cardiovascular anomalies [NCBI] 6.30979e-05
TFAP2C [NCBI] 5.91221e-05
TFAP2A [NCBI] 5.91221e-05
EVC [NCBI] 5.21871e-05
ehlers-danlos syndrome, type iv, autosomal dominant [NCBI] 5.21871e-05
RA [NCBI] 5.0855e-05
CMTC [NCBI] 4.95223e-05
contractural arachnodactyly, congenital [NCBI] 4.2003e-05
AVSD [NCBI] 3.97289e-05
PTGS2 [NCBI] 3.63833e-05
ZS [NCBI] 3.43278e-05
SERPINA6 [NCBI] 3.18334e-05
phenylketonuria [NCBI] 2.42154e-05
AVP [NCBI] 2.36444e-05
MFS [NCBI] 2.30844e-05
MPO [NCBI] 1.92482e-05
PWS [NCBI] 9.60237e-06



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