Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Puerperal Disorders [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.000105673
F5 [NCBI] 5.07387e-05
TPO [NCBI] 4.67389e-05
F2 [NCBI] 4.39625e-05
PRL [NCBI] 2.74861e-05
PIH [NCBI] 1.9508e-05
PTHLH [NCBI] 1.5643e-05
HTR2A [NCBI] 1.51962e-05
TG [NCBI] 1.46502e-05
GLRA2 [NCBI] 1.42428e-05
SLC6A4 [NCBI] 9.97225e-06
TRH [NCBI] 8.52715e-06
TNF [NCBI] 8.18069e-06
HTR2C [NCBI] 7.92495e-06
AVP [NCBI] 7.70858e-06
MTHFR [NCBI] 7.69853e-06
SERPINC1 [NCBI] 7.68018e-06
CTSD [NCBI] 7.44401e-06
PLTP [NCBI] 6.7629e-06
SLPI [NCBI] 6.26748e-06
NR3C1 [NCBI] 6.24561e-06
KCNQ1 [NCBI] 5.16323e-06
SLC5A5 [NCBI] 4.91068e-06
HP [NCBI] 4.82514e-06
TFPI [NCBI] 4.62488e-06
ENG [NCBI] 4.43192e-06
ESR1 [NCBI] 3.70659e-06
STAT3 [NCBI] 2.84222e-06
LPL [NCBI] 2.73371e-06
TGFB1 [NCBI] 2.0198e-06
FASLG [NCBI] 1.88487e-06
PTH [NCBI] 1.09706e-06



OMIM


 OMIM Link Information
gain		 01
carnitine deficiency, myopathic [NCBI] 0.000880362
restless legs syndrome, susceptibility to, 1 [NCBI] 0.000685
SLE [NCBI] 0.000129315
TPO [NCBI] 8.8496e-05
factor v deficiency [NCBI] 7.72982e-05
PRL [NCBI] 6.82416e-05
afibrinogenemia, congenital [NCBI] 6.67504e-05
carbamoyl phosphate synthetase i deficiency, hyperammonemia due to [NCBI] 6.58021e-05
TG [NCBI] 5.21076e-05
galactosemia [NCBI] 4.81951e-05
CMT1B [NCBI] 4.70281e-05
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 4.62069e-05
CLS [NCBI] 4.4928e-05
FGG [NCBI] 4.36596e-05
factor x deficiency [NCBI] 3.71474e-05
PCI [NCBI] 3.62808e-05
porphyria cutanea tarda [NCBI] 3.39018e-05
protein c deficiency, congenital thrombotic disease due to [NCBI] 3.32733e-05
SLPI [NCBI] 3.03996e-05
PCD [NCBI] 2.98783e-05
PLTP [NCBI] 2.88397e-05
LAM [NCBI] 2.84283e-05
CRH [NCBI] 2.13839e-05
LCAT [NCBI] 2.08611e-05
AVP [NCBI] 1.81869e-05
HP [NCBI] 1.80509e-05
TFPI [NCBI] 1.57896e-05
RA [NCBI] 1.28552e-05
FMF [NCBI] 1.13225e-05
CD [NCBI] 1.05023e-05
F3 [NCBI] 7.76044e-06
TNF [NCBI] 7.11949e-06
LPL [NCBI] 6.50008e-06
thrombocytopenic purpura, autoimmune [NCBI] 4.09581e-06
MG [NCBI] 2.12166e-06
PTH [NCBI] 2.46085e-07



Database Center for Life Science