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MeSH keywords -> Related genes, diseases (OMIM)


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01 Carrier State [NCBI]

Gene


 Gene Link Information
Gain		 01



OMIM


 OMIM Link Information
gain		 01
RP23 [NCBI] 0.00189937
CF [NCBI] 0.000458984
cirrhosis, familial [NCBI] 0.000141555
ruvalcaba syndrome [NCBI] 9.65415e-05
AFP [NCBI] 9.61737e-05
hunter-mcalpine craniosynostosis syndrome [NCBI] 9.14963e-05
ALD [NCBI] 8.88578e-05
hemochromatosis, neonatal [NCBI] 8.41415e-05
hepatitis b virus, susceptibility to [NCBI] 7.65789e-05
CMT4D [NCBI] 7.65789e-05
von willebrand disease, recessive form [NCBI] 7.27822e-05
IFNA1 [NCBI] 7.03577e-05
ICP [NCBI] 6.56311e-05
hepatitis c virus, susceptibility to [NCBI] 6.04118e-05
hepatocellular carcinoma [NCBI] 5.70608e-05
PARK2 [NCBI] 5.23195e-05
CTNS [NCBI] 4.95373e-05
aHUS [NCBI] 4.95373e-05
LAD [NCBI] 4.66655e-05
TNF [NCBI] 4.60929e-05
TMEM142C [NCBI] 4.25497e-05
TMEM142B [NCBI] 4.25497e-05
ND [NCBI] 3.94264e-05
SMA1 [NCBI] 3.64126e-05
CGD [NCBI] 3.54328e-05
TMEM142A [NCBI] 3.47185e-05
TLR2 [NCBI] 3.36703e-05
IL10RB [NCBI] 3.28717e-05
IFNAR2 [NCBI] 3.28717e-05
WHS [NCBI] 3.23828e-05
FFI [NCBI] 3.23828e-05
PDE11A [NCBI] 3.21273e-05
neuraminidase deficiency with beta-galactosidase deficiency [NCBI] 2.41726e-05
PTPRC [NCBI] 2.30201e-05
SMN2 [NCBI] 2.27285e-05
ITGB2 [NCBI] 2.10152e-05
leber optic atrophy [NCBI] 2.06753e-05
SMN1 [NCBI] 1.79559e-05
HNF1A [NCBI] 1.78937e-05
GCK [NCBI] 1.78322e-05
CJD [NCBI] 1.63854e-05
von willebrand disease [NCBI] 1.60595e-05
VDR [NCBI] 1.37379e-05
DMD [NCBI] 1.33723e-05
PLG [NCBI] 1.26724e-05
HP [NCBI] 8.77785e-06
APOE [NCBI] 8.30489e-06
IL2 [NCBI] 7.94572e-06
PTHLH [NCBI] 6.66855e-06
RA [NCBI] 6.08299e-06
TF [NCBI] 6.07363e-06
SHBG [NCBI] 5.27381e-06
AD [NCBI] 4.53889e-06
CD [NCBI] 4.45975e-06
TNFSF6 [NCBI] 3.43996e-06
SLE [NCBI] 2.90234e-06
LPL [NCBI] 1.94767e-06
VEGF [NCBI] 1.37036e-06
AR [NCBI] 1.09988e-06
ACHE [NCBI] 3.41075e-07
MG [NCBI] 9.11324e-08



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