Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Vomiting [NCBI]

Gene


 Gene Link Information
Gain		 01
GER [NCBI] 0.0052837
MS [NCBI] 0.000442074
BULN [NCBI] 0.000295835
GTS [NCBI] 5.91577e-05
HTR3C [NCBI] 3.25129e-05
FAAH [NCBI] 2.75518e-05
HTR3B [NCBI] 2.47887e-05
DPP4 [NCBI] 2.20104e-05
TRH [NCBI] 2.03126e-05
TACR1 [NCBI] 2.02738e-05
AVP [NCBI] 1.86504e-05
CCK [NCBI] 1.34815e-05
UGT1A1 [NCBI] 1.17117e-05
CHGA [NCBI] 1.13769e-05
MAP4 [NCBI] 1.10683e-05
CYP3A4 [NCBI] 1.07296e-05
ABCB1 [NCBI] 1.00883e-05
NFAT5 [NCBI] 1.00589e-05
PRL [NCBI] 9.06858e-06
NAGS [NCBI] 8.96814e-06
DNAJA1 [NCBI] 8.77752e-06
TAC1 [NCBI] 8.05335e-06
CALCA [NCBI] 7.89277e-06
PTH1R [NCBI] 7.60605e-06
CYP2C8 [NCBI] 7.4611e-06
ACHE [NCBI] 7.04746e-06
TPMT [NCBI] 6.95945e-06
SERPING1 [NCBI] 6.52416e-06
CYP1A2 [NCBI] 6.20462e-06
TNFRSF1A [NCBI] 5.99353e-06
TYMS [NCBI] 5.60938e-06
CYP2D6 [NCBI] 5.53677e-06
PYY [NCBI] 5.37604e-06
DRD4 [NCBI] 5.20749e-06
CYP2C19 [NCBI] 4.84877e-06
CYP2C9 [NCBI] 4.79686e-06
CD99 [NCBI] 4.76871e-06
ERCC1 [NCBI] 4.72465e-06
PDE5A [NCBI] 4.63995e-06
GDNF [NCBI] 4.61945e-06
PROM1 [NCBI] 4.5992e-06
PRKCA [NCBI] 4.53991e-06
KRT7 [NCBI] 4.35227e-06
TNF [NCBI] 3.8915e-06
TOP2A [NCBI] 3.83575e-06
TROVE2 [NCBI] 3.80477e-06
COMT [NCBI] 3.69517e-06
FOXP3 [NCBI] 3.54523e-06
SLC6A4 [NCBI] 3.45192e-06
GSTP1 [NCBI] 2.94624e-06
MTHFR [NCBI] 2.36824e-06
PTEN [NCBI] 2.19657e-06
BAX [NCBI] 1.65354e-06
GFAP [NCBI] 1.60783e-06
PTH [NCBI] 8.23082e-07
PTGS2 [NCBI] 8.20402e-07



OMIM


 OMIM Link Information
gain		 01
CVS [NCBI] 0.00444795
pyloric atresia [NCBI] 0.00190762
ANON1 [NCBI] 0.000773718
BULN1 [NCBI] 0.000724991
visceral neuropathy, familial, autosomal recessive [NCBI] 0.000705355
megaduodenum and/or megacystis [NCBI] 0.000601551
migraine with or without aura, susceptibility to, 1 [NCBI] 0.000533713
colloid cysts of third ventricle [NCBI] 0.000148656
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 0.000146808
FAAH [NCBI] 0.000127597
SLE [NCBI] 0.000120736
enteropathy, familial, with villous edema and immunoglobulin g2 deficiency [NCBI] 0.000112819
RA [NCBI] 8.35352e-05
AVP [NCBI] 7.28923e-05
lactose intolerance, congenital [NCBI] 7.23215e-05
n-acetylglutamate synthase deficiency [NCBI] 6.63736e-05
PWS [NCBI] 6.46305e-05
CDG1B [NCBI] 6.02593e-05
CNR2 [NCBI] 5.9004e-05
MAP4 [NCBI] 5.6495e-05
IHPS1 [NCBI] 5.34768e-05
NAGS [NCBI] 5.28343e-05
carbamoyl phosphate synthetase i deficiency, hyperammonemia due to [NCBI] 5.04733e-05
propionic acidemia [NCBI] 4.79537e-05
pyruvate carboxylase deficiency [NCBI] 4.6475e-05
acyl-coa dehydrogenase, medium-chain, deficiency of [NCBI] 4.57853e-05
MTP [NCBI] 4.55804e-05
IVA [NCBI] 4.38833e-05
MELAS [NCBI] 4.38833e-05
SLC12A3 [NCBI] 4.35931e-05
biotinidase deficiency [NCBI] 4.32981e-05
hyperglycerolemia [NCBI] 4.32981e-05
ATRX [NCBI] 4.27344e-05
CCK [NCBI] 4.20923e-05
bartter syndrome, type 3 [NCBI] 4.11577e-05
MEN2B [NCBI] 4.06664e-05
ACADS [NCBI] 4.00961e-05
fructose intolerance, hereditary [NCBI] 3.54883e-05
CF [NCBI] 3.17292e-05
ABL [NCBI] 3.10215e-05
OXT [NCBI] 3.09594e-05
CRC [NCBI] 3.02501e-05
tyrosinemia, type i [NCBI] 2.98729e-05
MTTL1 [NCBI] 2.80121e-05
LPI [NCBI] 2.74627e-05
TYMS [NCBI] 2.56848e-05
IFNA1 [NCBI] 2.34946e-05
PYY [NCBI] 1.94113e-05
PRL [NCBI] 1.91717e-05
ACHE [NCBI] 1.7971e-05
DMD [NCBI] 1.47749e-05
CPI [NCBI] 1.36142e-05
PJS [NCBI] 1.25683e-05
GDNF [NCBI] 1.07312e-05
AD [NCBI] 7.53485e-06
GTS [NCBI] 5.40265e-06
CRH [NCBI] 3.06385e-06
TNF [NCBI] 2.65539e-06
KLK3 [NCBI] 2.59474e-06
FMF [NCBI] 1.80585e-06
VEGF [NCBI] 1.50684e-06
GFAP [NCBI] 1.03284e-06
PD [NCBI] 3.40054e-07
thrombocytopenic purpura, autoimmune [NCBI] 1.91348e-07
PTH [NCBI] 3.77539e-08



Database Center for Life Science