Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Remission, Spontaneous [NCBI]


Gene


Gene Link Information
Gain
01
MS [NCBI] 0.002167443
VUR [NCBI] 0.000810072
TEC [NCBI] 0.000370636
IGHE [NCBI] 0.0002072193
BFIC [NCBI] 0.0001971181
PKC [NCBI] 0.0001391011
PPR [NCBI] 0.0001322628
GTS [NCBI] 8.72005e-05
MBP [NCBI] 3.534016e-05
GNRHR [NCBI] 2.073786e-05
FLVCR2 [NCBI] 1.887219e-05
SCN4B [NCBI] 1.638422e-05
CD68 [NCBI] 1.516647e-05
NEFH [NCBI] 1.447019e-05
STX11 [NCBI] 1.390052e-05
LAMB3 [NCBI] 1.313447e-05
PTH [NCBI] 1.307486e-05
PDLIM4 [NCBI] 1.304788e-05
GJB1 [NCBI] 1.278722e-05
ARTN [NCBI] 1.254555e-05
CCR2 [NCBI] 1.240376e-05
IGAN [NCBI] 1.1810172e-05
NTF3 [NCBI] 1.169597e-05
AFP [NCBI] 1.156983e-05
MOG [NCBI] 1.121481e-05
ADAMTS4 [NCBI] 1.117317e-05
SEPT9 [NCBI] 1.055925e-05
GER [NCBI] 1.053278e-05
INDO [NCBI] 1.033482e-05
MX1 [NCBI] 1.028011e-05
SGCE [NCBI] 1.010479e-05
ADA [NCBI] 1.004384e-05
FCER1A [NCBI] 1.002009e-05
PTHLH [NCBI] 9.95807e-06
PRAME [NCBI] 9.90223e-06
SLC25A13 [NCBI] 9.82631e-06
ECM1 [NCBI] 9.78802e-06
PTPRN2 [NCBI] 9.50692e-06
KISS1R [NCBI] 8.91432e-06
ENO1 [NCBI] 8.89253e-06
ITGB4 [NCBI] 8.75481e-06
CD48 [NCBI] 8.75377e-06
TRH [NCBI] 8.74954e-06
RNASE3 [NCBI] 8.72277e-06
CDKN2C [NCBI] 8.5922e-06
ADAMTS2 [NCBI] 8.41683e-06
ID2 [NCBI] 8.31567e-06
IKBKG [NCBI] 8.09945e-06
KAL1 [NCBI] 8.06553e-06
TGM1 [NCBI] 7.74364e-06
IL12B [NCBI] 7.47704e-06
CD79A [NCBI] 7.46638e-06
CCR1 [NCBI] 7.25552e-06
TIMP1 [NCBI] 7.12329e-06
HGF [NCBI] 7.03487e-06
PIGA [NCBI] 6.9729e-06
ENPP1 [NCBI] 6.96757e-06
CXCL9 [NCBI] 6.8136e-06
CRH [NCBI] 6.80508e-06
CCR4 [NCBI] 6.7376e-06
ABL1 [NCBI] 6.69935e-06
TFF2 [NCBI] 6.5417e-06
CXCL10 [NCBI] 6.43958e-06
SERPINA1 [NCBI] 6.38e-06
GATA1 [NCBI] 6.14108e-06
MYCN [NCBI] 6.1249e-06
CYBA [NCBI] 6.10825e-06
CCR3 [NCBI] 6.01394e-06
VWF [NCBI] 6.00944e-06
FGF23 [NCBI] 5.99929e-06
CCL5 [NCBI] 5.95352e-06
TAP2 [NCBI] 5.87783e-06
CCR7 [NCBI] 5.83049e-06
FASLG [NCBI] 5.82357e-06
IRF1 [NCBI] 5.79681e-06
SCGB1A1 [NCBI] 5.73445e-06
ETV6 [NCBI] 5.7188e-06
CREBBP [NCBI] 5.62963e-06
GDNF [NCBI] 5.42877e-06
ALK [NCBI] 5.33637e-06
TAP1 [NCBI] 5.26752e-06
MUC2 [NCBI] 5.26329e-06
CXCR3 [NCBI] 5.23667e-06
PIH [NCBI] 5.07264e-06
PMP22 [NCBI] 5.02505e-06
GZMB [NCBI] 4.86572e-06
CCR5 [NCBI] 4.77699e-06
SLC2A1 [NCBI] 4.72748e-06
TROVE2 [NCBI] 4.5743e-06
RUNX1 [NCBI] 4.46032e-06
FOXP3 [NCBI] 4.13224e-06
MLL [NCBI] 4.08842e-06
CCL2 [NCBI] 3.80238e-06
SLC6A4 [NCBI] 3.727194e-06
IL10 [NCBI] 3.31554e-06
ACE [NCBI] 3.08736e-06
CASP9 [NCBI] 3.047656e-06
VIP [NCBI] 2.947973e-06
BIRC5 [NCBI] 2.768088e-06
BCL2L1 [NCBI] 2.706318e-06
IL6 [NCBI] 2.699804e-06
TNFSF10 [NCBI] 2.57303e-06
LPL [NCBI] 2.569388e-06
TH [NCBI] 2.483643e-06
IL1RN [NCBI] 2.417953e-06
TGFB1 [NCBI] 1.821383e-06
BAX [NCBI] 1.74699e-06
MPO [NCBI] 1.723765e-06
TNF [NCBI] 1.55178e-06
PRL [NCBI] 1.285798e-06
CDKN1A [NCBI] 1.003741e-06




OMIM


OMIM Link Information
gain
01
EKD1 [NCBI] 0.0011991
pulmonary alveolar proteinosis, acquired [NCBI] 0.000801832
VUR1 [NCBI] 0.000593468
thrombocytopenia-absent radius syndrome [NCBI] 0.000593468
myeloproliferative syndrome, transient [NCBI] 0.000543053
PPR [NCBI] 0.000481279
thrombocytopenic purpura, autoimmune [NCBI] 0.000426468
GACI [NCBI] 0.000143559
fertile eunuch syndrome [NCBI] 0.000133162
aniridia, microcornea, and spontaneously reabsorbed cataract [NCBI] 0.000133162
ankyloblepharon filiforme adnatum and cleft palate [NCBI] 0.000105414
panencephalitis, subacute sclerosing [NCBI] 9.65364e-05
CEACAM5 [NCBI] 9.41371e-05
FHL4 [NCBI] 8.81752e-05
seizures, benign familial neonatal-infantile [NCBI] 8.31389e-05
ectodermal dysplasia, hypohidrotic, with immune deficiency [NCBI] 7.91307e-05
PDV [NCBI] 7.58018e-05
citrullinemia, type ii, neonatal-onset [NCBI] 7.29558e-05
GGM [NCBI] 7.04708e-05
GTS [NCBI] 6.90196e-05
CTLN2 [NCBI] 6.8266e-05
osteoporosis, juvenile [NCBI] 6.44872e-05
RA [NCBI] 6.23207e-05
BHC [NCBI] 5.99184e-05
propionic acidemia [NCBI] 5.99184e-05
alexander disease [NCBI] 5.86077e-05
CF [NCBI] 5.83608e-05
NPHS1 [NCBI] 5.73806e-05
MBP [NCBI] 5.71123e-05
GABEB [NCBI] 5.62273e-05
epidermolysis bullosa with pyloric atresia [NCBI] 5.22058e-05
SEDC [NCBI] 4.96662e-05
citrullinemia, classic [NCBI] 4.96662e-05
porphyria, acute intermittent [NCBI] 3.90958e-05
STX11 [NCBI] 3.37934e-05
MG [NCBI] 3.3719e-05
temporal arteritis [NCBI] 3.21092e-05
IL12RB2 [NCBI] 3.1947e-05
SLC25A13 [NCBI] 3.1947e-05
MAF [NCBI] 3.12028e-05
MIRN16-1 [NCBI] 3.12028e-05
hypogonadotropic hypogonadism [NCBI] 3.07479e-05
PSORS1 [NCBI] 2.84381e-05
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency [NCBI] 2.77352e-05
ITGB4 [NCBI] 2.65867e-05
LAMB3 [NCBI] 2.51699e-05
DBA [NCBI] 2.40657e-05
IL12B [NCBI] 2.30738e-05
IKBKG [NCBI] 2.27315e-05
PIGA [NCBI] 2.25676e-05
transcobalamin ii deficiency [NCBI] 2.19542e-05
GNRHR [NCBI] 1.97907e-05
DNTT [NCBI] 1.91277e-05
RNASE3 [NCBI] 1.83044e-05
AFP [NCBI] 1.68135e-05
GJB1 [NCBI] 1.54329e-05
ADA [NCBI] 1.53931e-05
PTH [NCBI] 1.45099e-05
SLE [NCBI] 1.3459e-05
ALK [NCBI] 1.24593e-05
lymphoma, non-hodgkin, familial [NCBI] 1.19629e-05
AVP [NCBI] 1.08641e-05
MDD [NCBI] 9.47558e-06
HGF [NCBI] 7.11487e-06
hla-d histocompatibility type [NCBI] 6.87869e-06
SLC6A3 [NCBI] 5.45391e-06
VEGF [NCBI] 4.07835e-06
FMF [NCBI] 2.2172e-06
LPL [NCBI] 1.41506e-06
CD [NCBI] 9.87447e-07
MPO [NCBI] 9.08579e-07
VIP [NCBI] 5.27042e-07
TH [NCBI] 1.41352e-07
PRL [NCBI] 5.03076e-08
TNF [NCBI] 2.80443e-08




Database Center for Life Science