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MeSH keywords -> Related genes, diseases (OMIM)


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01 Heart Septal Defects, Ventricular [NCBI]


Gene


Gene Link Information
Gain
01
ACF [NCBI] 0.000340315
GER [NCBI] 9.91295e-05
CRELD1 [NCBI] 5.9725e-05
NKX2-5 [NCBI] 4.16496e-05
HEY2 [NCBI] 2.68702e-05
PTPN11 [NCBI] 2.31618e-05
JAG1 [NCBI] 1.59049e-05
UNC84B [NCBI] 1.42215e-05
SLC26A7 [NCBI] 1.42215e-05
SLC26A8 [NCBI] 1.36381e-05
SOX18 [NCBI] 1.19187e-05
EVC [NCBI] 1.1078e-05
INVS [NCBI] 1.04383e-05
SCN2A [NCBI] 1.04383e-05
TBX5 [NCBI] 1.01575e-05
TFAP2B [NCBI] 9.97355e-06
NFATC1 [NCBI] 9.75544e-06
NOS3 [NCBI] 9.20901e-06
TBX1 [NCBI] 9.08598e-06
FOXC2 [NCBI] 8.52933e-06
SCN1A [NCBI] 8.36269e-06
FGA [NCBI] 8.23176e-06
GLI1 [NCBI] 8.09071e-06
F13A1 [NCBI] 7.66506e-06
NAIP [NCBI] 7.57698e-06
BMP4 [NCBI] 6.48575e-06
SELPLG [NCBI] 6.43392e-06
ADM [NCBI] 6.39074e-06
CLU [NCBI] 5.93309e-06
EGR1 [NCBI] 5.68215e-06
TFPI [NCBI] 5.48459e-06
F8 [NCBI] 5.43161e-06
F2 [NCBI] 5.05952e-06
F5 [NCBI] 4.70618e-06
ACE [NCBI] 3.87999e-06
MTHFR [NCBI] 3.53392e-06
TNF [NCBI] 3.51304e-06
NOS2 [NCBI] 3.22641e-06
VEGFA [NCBI] 2.52952e-06




OMIM


OMIM Link Information
gain
01
AVSD [NCBI] 0.00261483
FRNS [NCBI] 0.00110591
patent ductus arteriosus [NCBI] 0.000764597
acanthosis nigricans [NCBI] 0.000693453
tibia, hypoplasia of, with polydactyly [NCBI] 0.000607858
cayler cardiofacial syndrome [NCBI] 0.000480827
AOS [NCBI] 0.000383542
kabuki syndrome [NCBI] 0.00034134
asplenia with cardiovascular anomalies [NCBI] 0.000293635
HEY2 [NCBI] 0.000252393
aneurysm of interventricular septum [NCBI] 0.000196473
AVSD2 [NCBI] 0.000172907
EVC [NCBI] 0.000170489
CRELD1 [NCBI] 0.000163492
CMH [NCBI] 0.000157874
heart, malformation of [NCBI] 0.000113606
cardiac septal defects with coarctation of the aorta [NCBI] 0.000113606
cranioacrofacial syndrome [NCBI] 0.000113606
distichiasis with congenital anomalies of the heart and peripheral vasculature [NCBI] 0.000113606
gonadal dysgenesis, xy type, with associated anomalies [NCBI] 0.000113606
pulmonary atresia with ventricular septal defect [NCBI] 0.000113606
aortic arch interruption, facial palsy, and retinal coloboma [NCBI] 9.11475e-05
craniosynostosis-mental retardation syndrome of lin and gettig [NCBI] 9.11475e-05
stratton-parker syndrome [NCBI] 9.11475e-05
HOS [NCBI] 8.55726e-05
mental retardation, buenos aires type [NCBI] 8.26799e-05
heterotaxy, visceral, 2, autosomal [NCBI] 7.71861e-05
right ventricular hypoplasia, isolated [NCBI] 7.31047e-05
weyers acrofacial dysostosis [NCBI] 6.98552e-05
lujan-fryns syndrome [NCBI] 6.48462e-05
emanuel syndrome [NCBI] 6.28292e-05
atrial septal defect with atrioventricular conduction defects [NCBI] 6.28292e-05
RXRA [NCBI] 6.23732e-05
MCOPS9 [NCBI] 5.94297e-05
HTX1 [NCBI] 5.79685e-05
CTHM [NCBI] 5.42527e-05
cerebrocostomandibular syndrome [NCBI] 5.42527e-05
PFM [NCBI] 5.42527e-05
tetralogy of fallot [NCBI] 5.31858e-05
DGS [NCBI] 5.15176e-05
seckel syndrome 1 [NCBI] 5.1247e-05
papillorenal syndrome [NCBI] 5.1247e-05
DRRS [NCBI] 5.1247e-05
PTPN11 [NCBI] 5.04881e-05
EDN1 [NCBI] 5.00371e-05
PAX2 [NCBI] 5.00371e-05
contractural arachnodactyly, congenital [NCBI] 4.52417e-05
andersen cardiodysrhythmic periodic paralysis [NCBI] 4.35001e-05
MKKS [NCBI] 4.24297e-05
ODDD [NCBI] 4.00416e-05
TBS [NCBI] 3.96058e-05
charge syndrome [NCBI] 3.91822e-05
cardiofaciocutaneous syndrome [NCBI] 3.79783e-05
SERPINA6 [NCBI] 3.5045e-05
CES [NCBI] 3.42435e-05
costello syndrome [NCBI] 3.3655e-05
BPES [NCBI] 3.30892e-05
ADM [NCBI] 3.07695e-05
GJA1 [NCBI] 3.02297e-05
AMC [NCBI] 2.98673e-05
SVAS [NCBI] 2.70569e-05
NS1 [NCBI] 2.45677e-05
TFPI [NCBI] 2.1804e-05
TNF [NCBI] 7.53248e-06
PWS [NCBI] 1.59835e-06
thrombocytopenic purpura, autoimmune [NCBI] 8.60451e-08




Database Center for Life Science