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MeSH keywords -> Related genes, diseases (OMIM)


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01 Cortisone [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.000167687
HSD11B1 [NCBI] 6.69351e-05
HSD11B2 [NCBI] 5.27083e-05
CYP7B1 [NCBI] 3.7394e-06
NR3C2 [NCBI] 3.34736e-06
SI [NCBI] 3.09261e-06
TAT [NCBI] 2.58458e-06
GHR [NCBI] 2.53844e-06
CRH [NCBI] 2.46857e-06
EGF [NCBI] 2.1559e-06
AKR1D1 [NCBI] 2.11003e-06
SDS [NCBI] 2.04672e-06
AADAC [NCBI] 2.01992e-06
PRL [NCBI] 1.8137e-06
H6PD [NCBI] 1.80435e-06
SRD5A1 [NCBI] 1.63969e-06
SPIB [NCBI] 1.58437e-06
HSD3B2 [NCBI] 1.58437e-06
PTGER2 [NCBI] 1.51062e-06
HSD17B1 [NCBI] 1.50315e-06
NR0B1 [NCBI] 1.4888e-06
TRH [NCBI] 1.45582e-06
TNF [NCBI] 1.29085e-06
PTGER1 [NCBI] 1.17335e-06
PLTP [NCBI] 1.16911e-06
PIH [NCBI] 1.14122e-06
NPY [NCBI] 1.13136e-06
MYOC [NCBI] 1.08442e-06
ETV6 [NCBI] 1.08366e-06
IAPP [NCBI] 1.0535e-06
NR3C1 [NCBI] 1.03963e-06
PTH [NCBI] 1.03899e-06
GIP [NCBI] 9.57851e-07
IBSP [NCBI] 9.43179e-07
BCR [NCBI] 9.37882e-07
RUNX1 [NCBI] 9.11313e-07
SERPINE1 [NCBI] 8.8505e-07
EGR1 [NCBI] 8.84694e-07
NR1H3 [NCBI] 8.67791e-07
PTHLH [NCBI] 7.56591e-07
CETP [NCBI] 7.29438e-07
CYP3A4 [NCBI] 6.30977e-07
STAT3 [NCBI] 6.10103e-07
MBP [NCBI] 5.55502e-07
AFP [NCBI] 5.3486e-07
AR [NCBI] 4.99704e-07
AVP [NCBI] 4.83869e-07
GFAP [NCBI] 4.76928e-07
ACHE [NCBI] 4.19952e-07
CDKN1A [NCBI] 3.97343e-07
PTGS2 [NCBI] 3.68483e-07
NGF [NCBI] 3.36148e-07



OMIM


 OMIM Link Information
gain		 01
keratitis fugax hereditaria [NCBI] 0.00264194
adrenal unresponsiveness to acth [NCBI] 0.00192174
PCOS1 [NCBI] 0.000971445
cortisol 11-beta-ketoreductase deficiency [NCBI] 0.000616456
cortisone reductase deficiency [NCBI] 0.000599369
AME2 [NCBI] 0.00027869
AHC [NCBI] 0.000181464
periodic fever, familial, autosomal dominant [NCBI] 0.000164973
ataxic diplegia with defective cellular immunity [NCBI] 0.00013902
CPI [NCBI] 0.000128014
VRNI [NCBI] 9.50198e-05
HNA [NCBI] 9.22995e-05
camurati-engelmann disease [NCBI] 8.70523e-05
GCCD1 [NCBI] 8.55445e-05
corticosterone methyloxidase type ii deficiency [NCBI] 8.4132e-05
pituitary dwarfism iii [NCBI] 8.28033e-05
adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiency [NCBI] 7.92347e-05
HSD11B1 [NCBI] 5.33462e-05
thrombasthenia of glanzmann and naegeli [NCBI] 4.9367e-05
DBA [NCBI] 4.77643e-05
SI [NCBI] 3.50686e-05
HPGD [NCBI] 3.11706e-05
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [NCBI] 2.94846e-05
AT [NCBI] 2.79916e-05
lipase, congenital absence of pancreatic [NCBI] 2.71672e-05
SLE [NCBI] 2.64886e-05
GHR [NCBI] 2.57473e-05
SERPINA6 [NCBI] 2.52515e-05
ALD [NCBI] 2.27629e-05
CYP11B1 [NCBI] 2.14966e-05
CYP11B2 [NCBI] 2.02912e-05
PHEX [NCBI] 1.98485e-05
glycogen storage disease i [NCBI] 1.88233e-05
CF [NCBI] 1.81336e-05
CRH [NCBI] 1.58552e-05
H6PD [NCBI] 1.51991e-05
RA [NCBI] 1.34651e-05
BGLAP [NCBI] 1.13966e-05
CD [NCBI] 1.09309e-05
PLTP [NCBI] 1.05299e-05
IAPP [NCBI] 8.52892e-06
STAT3 [NCBI] 7.90935e-06
GIP [NCBI] 6.16834e-06
hla-d histocompatibility type [NCBI] 6.0425e-06
CYP1A1 [NCBI] 5.76346e-06
thrombocytopenic purpura, autoimmune [NCBI] 4.59545e-06
VEGF [NCBI] 3.41756e-06
GNRH1 [NCBI] 3.2721e-06
PRL [NCBI] 2.725e-06
AVP [NCBI] 1.9667e-06
EGF [NCBI] 1.39701e-06
NPY [NCBI] 1.11552e-06
NGFB [NCBI] 6.12411e-07
PTH [NCBI] 5.24419e-07
MBP [NCBI] 5.16464e-07
AR [NCBI] 3.74817e-07
AFP [NCBI] 3.48966e-07
TNF [NCBI] 7.63324e-08
GFAP [NCBI] 5.25921e-08
ACHE [NCBI] 2.02148e-08



Database Center for Life Science