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MeSH keywords -> Related genes, diseases (OMIM)


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01 Mass Screening [NCBI]


Gene


Gene Link Information
Gain
01




OMIM


OMIM Link Information
gain
01
CRC [NCBI] 0.0152034
KLK3 [NCBI] 0.00714998
IS1 [NCBI] 0.00157957
panic disorder 2 [NCBI] 0.00114987
aneurysm, intracranial berry, 1 [NCBI] 0.00109455
RA [NCBI] 0.000983515
AFP [NCBI] 0.00082972
CD [NCBI] 0.000756119
CNA1 [NCBI] 0.000720912
iminoglycinuria [NCBI] 0.000576422
PAND1 [NCBI] 0.000453401
chiari malformation type i [NCBI] 0.000398996
SLE [NCBI] 0.000326856
APC [NCBI] 0.000306219
apnea, obstructive sleep [NCBI] 0.000302292
histidinemia [NCBI] 0.000257457
cystathioninuria [NCBI] 0.000186173
MDD [NCBI] 0.000151463
MAFD6 [NCBI] 0.000150188
CHNG2 [NCBI] 0.000116139
biotinidase deficiency [NCBI] 0.00011356
IDDM [NCBI] 9.94356e-05
VEGF [NCBI] 9.62982e-05
EGF [NCBI] 9.56988e-05
methionine adenosyltransferase deficiency [NCBI] 8.11039e-05
TSD [NCBI] 7.98112e-05
CEACAM5 [NCBI] 7.5893e-05
hartnup disorder [NCBI] 7.56752e-05
CJD [NCBI] 7.14438e-05
ACPP [NCBI] 6.28128e-05
G6PD [NCBI] 6.2043e-05
AD [NCBI] 5.70956e-05
hydroxyprolinemia [NCBI] 5.25135e-05
costello syndrome [NCBI] 4.79711e-05
HFE [NCBI] 4.38432e-05
sarcosinemia [NCBI] 4.37329e-05
LGMD2F [NCBI] 4.37329e-05
pancreatic cancer, susceptibility to, 1 [NCBI] 4.0536e-05
PRL [NCBI] 3.91115e-05
phenylketonuria [NCBI] 3.88156e-05
MAT1A [NCBI] 3.75297e-05
PD [NCBI] 3.6579e-05
neuroblastoma [NCBI] 3.5633e-05
galactosemia [NCBI] 3.49288e-05
GRA [NCBI] 3.42427e-05
PCNA [NCBI] 3.40037e-05
LGMD2E [NCBI] 3.3396e-05
CTLN2 [NCBI] 3.3396e-05
schwannomatosis [NCBI] 3.3396e-05
galactokinase deficiency [NCBI] 3.1547e-05
carnitine palmitoyltransferase ii deficiency, late-onset [NCBI] 2.9881e-05
galactose epimerase deficiency [NCBI] 2.83674e-05
TWISTNB [NCBI] 2.75189e-05
FMF [NCBI] 2.70409e-05
PG [NCBI] 2.69552e-05
aspartylglucosaminuria [NCBI] 2.57353e-05
BDNF [NCBI] 2.4325e-05
CRH [NCBI] 2.38937e-05
PHA [NCBI] 2.34342e-05
mucopolysaccharidosis type iiia [NCBI] 2.34342e-05
tyrosinemia, type i [NCBI] 2.2964e-05
ACHE [NCBI] 2.26353e-05
HRPT1 [NCBI] 2.14571e-05
PCLD [NCBI] 2.14571e-05
KTCN1 [NCBI] 2.05601e-05
HBD [NCBI] 2.00064e-05
COH1 [NCBI] 1.97416e-05
ETM1 [NCBI] 1.97158e-05
aortic aneurysm, abdominal [NCBI] 1.89192e-05
MPO [NCBI] 1.83195e-05
methylmalonic aciduria due to methylmalonyl-coa mutase deficiency [NCBI] 1.81661e-05
acyl-coa dehydrogenase, medium-chain, deficiency of [NCBI] 1.74526e-05
SLOS [NCBI] 1.69388e-05
lung cancer [NCBI] 1.61318e-05
BRCA1 [NCBI] 1.49744e-05
usher syndrome, type i [NCBI] 1.49346e-05
FOXE1 [NCBI] 1.40987e-05
hypophosphatasia, infantile [NCBI] 1.38436e-05
PTH [NCBI] 1.35739e-05
ADHD [NCBI] 1.35252e-05
SGCA [NCBI] 1.3359e-05
LGMD2C [NCBI] 1.33336e-05
ALD [NCBI] 1.28612e-05
PTS [NCBI] 1.27073e-05
CVS [NCBI] 1.23768e-05
CMH [NCBI] 1.23201e-05
phenylketonuria ii [NCBI] 1.21257e-05
GJB6 [NCBI] 1.18569e-05
GFER [NCBI] 1.11235e-05
LDHB [NCBI] 1.06859e-05
COH1 [NCBI] 1.06827e-05
lactase persistence [NCBI] 1.06827e-05
APOE [NCBI] 1.01091e-05
melanoma, uveal [NCBI] 9.92968e-06
DPYD [NCBI] 9.73052e-06
POAG [NCBI] 9.57382e-06
ACADM [NCBI] 9.50184e-06
F3 [NCBI] 9.09623e-06
LTA [NCBI] 8.6389e-06
ACADS [NCBI] 8.6389e-06
HBB [NCBI] 8.39116e-06
SCS [NCBI] 7.97534e-06
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [NCBI] 7.85993e-06
ENG [NCBI] 7.7473e-06
HBG2 [NCBI] 7.30446e-06
HS [NCBI] 6.99824e-06
VDR [NCBI] 6.82821e-06
GALT [NCBI] 6.80504e-06
MHS1 [NCBI] 6.6315e-06
maple syrup urine disease [NCBI] 6.6315e-06
PSEN2 [NCBI] 6.44213e-06
CFTR [NCBI] 5.94252e-06
hurler syndrome [NCBI] 5.70629e-06
GPT [NCBI] 5.64945e-06
MTHFR [NCBI] 4.63448e-06
PI [NCBI] 4.56469e-06
GBA [NCBI] 4.26332e-06
porphyria variegata [NCBI] 4.17782e-06
gaucher disease, type i [NCBI] 4.17782e-06
homocystinuria [NCBI] 4.01989e-06
MEN2A [NCBI] 4.01262e-06
MFS [NCBI] 3.87398e-06
LPI [NCBI] 3.85255e-06
AIRE [NCBI] 3.79246e-06
metachromatic leukodystrophy [NCBI] 3.69745e-06
PJS [NCBI] 3.57566e-06
LDLR [NCBI] 3.47552e-06
PCI [NCBI] 3.30311e-06
ADA [NCBI] 3.29637e-06
AVSD [NCBI] 3.26049e-06
BWS [NCBI] 3.00431e-06
ESD [NCBI] 2.78398e-06
lynch syndrome i [NCBI] 2.73896e-06
SHBG [NCBI] 2.71991e-06
HBA2 [NCBI] 2.6601e-06
breast cancer [NCBI] 2.61866e-06
SPP1 [NCBI] 2.54822e-06
BRCA2 [NCBI] 2.54165e-06
GAPDH [NCBI] 1.93253e-06
wilson disease [NCBI] 1.78547e-06
PSEN1 [NCBI] 1.73606e-06
TNFRSF11B [NCBI] 1.691e-06
TF [NCBI] 1.65529e-06
TTR [NCBI] 1.45301e-06
GJB2 [NCBI] 1.33181e-06
danubian endemic familial nephropathy [NCBI] 1.29321e-06
DMD [NCBI] 1.19e-06
APS1 [NCBI] 1.15127e-06
fabry disease [NCBI] 1.08417e-06
GTS [NCBI] 9.02755e-07
CD [NCBI] 8.97664e-07
FMR1 [NCBI] 8.92642e-07
ALB [NCBI] 8.4465e-07
HBA1 [NCBI] 4.03926e-07
hypercholesterolemia, autosomal dominant [NCBI] 3.84838e-07
TS [NCBI] 2.73501e-07
TG [NCBI] 1.68553e-07
CP [NCBI] 1.43809e-07
MBL2 [NCBI] 1.05867e-07
APOB [NCBI] 6.86103e-08
TPO [NCBI] 3.92389e-08
CF [NCBI] 1.77552e-08
LAM [NCBI] 1.75504e-08
PCD [NCBI] 1.75504e-08




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