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MeSH keywords -> Related genes, diseases (OMIM)


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01 Heart Septal Defects, Atrial [NCBI]


Gene


Gene Link Information
Gain
01
ASD1 [NCBI] 0.000438875
TARPS [NCBI] 0.000378131
NKX2-5 [NCBI] 0.000237274
GATA4 [NCBI] 8.13494e-05
CRELD1 [NCBI] 3.9841e-05
F2 [NCBI] 2.60012e-05
F5 [NCBI] 2.4566e-05
MYL7 [NCBI] 1.41473e-05
BMP4 [NCBI] 1.34417e-05
TLL1 [NCBI] 1.32489e-05
UNC84B [NCBI] 1.32489e-05
PTPN11 [NCBI] 1.20417e-05
ZFPM2 [NCBI] 1.07746e-05
MYH6 [NCBI] 1.07746e-05
HTR4 [NCBI] 1.06184e-05
EVC [NCBI] 1.01061e-05
SALL4 [NCBI] 9.39216e-06
ACTC1 [NCBI] 9.25211e-06
FAT1 [NCBI] 9.25211e-06
TBX5 [NCBI] 9.18616e-06
TFAP2B [NCBI] 9.00232e-06
ISL1 [NCBI] 8.45933e-06
TH [NCBI] 7.67822e-06
ATP1A2 [NCBI] 7.32715e-06
NOS3 [NCBI] 7.30823e-06
FGA [NCBI] 7.26309e-06
PAFAH1B1 [NCBI] 6.88849e-06
COL3A1 [NCBI] 6.80648e-06
MYH7 [NCBI] 6.69795e-06
F13A1 [NCBI] 6.69795e-06
NAIP [NCBI] 6.61017e-06
DBH [NCBI] 6.31049e-06
BMPR2 [NCBI] 6.21759e-06
TWIST1 [NCBI] 6.15114e-06
VWF [NCBI] 5.85316e-06
SELPLG [NCBI] 5.47271e-06
ADM [NCBI] 5.42982e-06
CACNA1A [NCBI] 5.388e-06
CLU [NCBI] 4.9758e-06
PDE5A [NCBI] 4.91782e-06
DMPK [NCBI] 4.88195e-06
CALCA [NCBI] 3.07327e-06
ACE [NCBI] 2.95962e-06
MTHFR [NCBI] 2.62583e-06
CFTR [NCBI] 1.35613e-06




OMIM


OMIM Link Information
gain
01
ASD1 [NCBI] 0.00727658
AVSD [NCBI] 0.00248322
axenfeld-rieger anomaly with cardiac defects and sensorineural hearing loss [NCBI] 0.00171781
atrial septal defect with atrioventricular conduction defects [NCBI] 0.000858821
TARPS [NCBI] 0.000785962
HOS [NCBI] 0.000526206
NKX2E [NCBI] 0.000512938
lymphedema, microcephaly, chorioretinopathy syndrome [NCBI] 0.000419401
DURS1 [NCBI] 0.000419401
dandy-walker-like malformation with atrioventricular septal defect [NCBI] 0.000384327
asplenia with cardiovascular anomalies [NCBI] 0.000291227
AOS [NCBI] 0.00027482
right ventricular hypoplasia, isolated [NCBI] 0.000171715
cardiofaciocutaneous syndrome [NCBI] 0.000166208
DRRS [NCBI] 0.000124673
lymphedema, atrial septal defect, and facial changes [NCBI] 0.000113012
brachydactyly, type e, with atrial septal defect, type ii [NCBI] 0.000113012
cardiac septal defects with coarctation of the aorta [NCBI] 0.000113012
pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities [NCBI] 0.000113012
atrial septal defect, secundum, with various cardiac and noncardiac defects [NCBI] 0.000113012
cardiac malformation, cleft lip-palate, microcephaly and digital anomalies [NCBI] 0.000113012
EVC [NCBI] 9.88932e-05
TLL1 [NCBI] 8.96982e-05
rapadilino syndrome [NCBI] 8.20878e-05
heterotaxy, visceral, 2, autosomal [NCBI] 7.65946e-05
AVSD2 [NCBI] 7.25138e-05
CRELD1 [NCBI] 7.07183e-05
emanuel syndrome [NCBI] 6.22404e-05
MYH6 [NCBI] 5.97434e-05
megalencephaly-cutis marmorata telangiectatica congenita [NCBI] 5.8842e-05
WSS [NCBI] 5.73814e-05
CRS1 [NCBI] 5.60441e-05
ACG2 [NCBI] 5.4811e-05
SALL4 [NCBI] 5.25308e-05
PQBP1 [NCBI] 5.19102e-05
seckel syndrome 1 [NCBI] 5.06632e-05
TRPS1 [NCBI] 4.6664e-05
weaver syndrome [NCBI] 4.59741e-05
contractural arachnodactyly, congenital [NCBI] 4.40399e-05
MKKS [NCBI] 4.1853e-05
fraser syndrome [NCBI] 4.13451e-05
MCOPS7 [NCBI] 4.08535e-05
TBS [NCBI] 3.90323e-05
charge syndrome [NCBI] 3.86093e-05
CES [NCBI] 3.36783e-05
costello syndrome [NCBI] 3.30909e-05
TH [NCBI] 3.30448e-05
CF [NCBI] 3.09147e-05
CLS [NCBI] 3.02262e-05
ADM [NCBI] 2.95844e-05
AMC [NCBI] 2.93114e-05
velocardiofacial syndrome [NCBI] 2.90915e-05
AVP [NCBI] 7.58292e-06
KLK3 [NCBI] 1.91382e-06
apnea, obstructive sleep [NCBI] 1.38274e-06
PWS [NCBI] 1.37912e-06
thrombocytopenic purpura, autoimmune [NCBI] 1.61473e-07




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