Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Transposition of Great Vessels [NCBI]


Gene


Gene Link Information
Gain
01
CFC1 [NCBI] 3.03187e-05
ZIC3 [NCBI] 2.91995e-05
NKX2-5 [NCBI] 2.34142e-05
MED13L [NCBI] 1.99659e-05
LEFTY1 [NCBI] 1.378e-05
INVS [NCBI] 1.29027e-05
NODAL [NCBI] 1.23804e-05
PITX1 [NCBI] 1.12046e-05
PITX3 [NCBI] 1.09915e-05




OMIM


OMIM Link Information
gain
01
splenic hypoplasia [NCBI] 0.00098052
short rib-polydactyly syndrome, type i [NCBI] 0.00092257
short rib-polydactyly syndrome, type ii [NCBI] 0.000785962
DTGA1 [NCBI] 0.000444944
HTX1 [NCBI] 0.000335568
ZIC3 [NCBI] 0.000268423
beemer lethal malformation syndrome [NCBI] 0.000146631
AVSD [NCBI] 0.000141421
heterotaxy, visceral, 2, autosomal [NCBI] 0.000110173
THRAP2 [NCBI] 0.00010573
situs inversus viscerum [NCBI] 9.7782e-05
CFC1 [NCBI] 9.19492e-05
CTHM [NCBI] 8.70992e-05
asplenia with cardiovascular anomalies [NCBI] 8.23042e-05
pheochromocytoma [NCBI] 7.4046e-05




Database Center for Life Science