Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Parathyroid Glands [NCBI]

Gene


 Gene Link Information
Gain		 01
PTH [NCBI] 0.00381245
HPT [NCBI] 0.00128034
CASR [NCBI] 0.000151453
VDR [NCBI] 0.000135086
PTHLH [NCBI] 4.60652e-05
FGF23 [NCBI] 4.51996e-05
MEN1 [NCBI] 3.62317e-05
GCM2 [NCBI] 3.61728e-05
CDC73 [NCBI] 3.41785e-05
CHGA [NCBI] 2.29878e-05
TBX1 [NCBI] 1.56496e-05
TBCE [NCBI] 1.33383e-05
SOX3 [NCBI] 1.08482e-05
LRP2 [NCBI] 1.07887e-05
PHEX [NCBI] 9.51828e-06
PAX1 [NCBI] 8.52629e-06
HOXA3 [NCBI] 8.43651e-06
PCNA [NCBI] 7.95215e-06
MEPE [NCBI] 7.11438e-06
NLRP5 [NCBI] 6.02594e-06
RET [NCBI] 5.95506e-06
COMMD5 [NCBI] 4.70955e-06
FGF8 [NCBI] 4.55897e-06
VAMP1 [NCBI] 4.06411e-06
CRABP1 [NCBI] 3.89063e-06
GATA3 [NCBI] 3.57965e-06
PHC1 [NCBI] 3.39999e-06
SLC20A1 [NCBI] 3.22391e-06
CITED2 [NCBI] 3.0749e-06
HOXD3 [NCBI] 3.0749e-06
TNF [NCBI] 3.07452e-06
CSDE1 [NCBI] 3.0082e-06
SOST [NCBI] 3.0082e-06
KHSRP [NCBI] 2.9765e-06
DLG2 [NCBI] 2.91608e-06
GNA11 [NCBI] 2.88723e-06
ADCYAP1 [NCBI] 2.85586e-06
PPP1R1B [NCBI] 2.75475e-06
PPP2R1B [NCBI] 2.70651e-06
CAPN2 [NCBI] 2.63845e-06
CCND1 [NCBI] 2.6149e-06
CYP27B1 [NCBI] 2.59564e-06
DLG3 [NCBI] 2.57495e-06
EYA1 [NCBI] 2.53487e-06
TP53BP2 [NCBI] 2.51545e-06
TSPO [NCBI] 2.51545e-06
PLCB2 [NCBI] 2.45949e-06
BMP3 [NCBI] 2.45949e-06
CHGB [NCBI] 2.38973e-06
RBP1 [NCBI] 2.37307e-06
DMP1 [NCBI] 2.35671e-06
SLC3A2 [NCBI] 2.34063e-06
EGFR [NCBI] 2.33914e-06
NKX2-1 [NCBI] 2.30705e-06
CDKN2C [NCBI] 2.26416e-06
RARB [NCBI] 2.23527e-06
FOXN1 [NCBI] 2.11542e-06
FGF3 [NCBI] 2.0207e-06
EGF [NCBI] 1.95908e-06
TFAM [NCBI] 1.89505e-06
APEX1 [NCBI] 1.88534e-06
DDC [NCBI] 1.87573e-06
CASP10 [NCBI] 1.84752e-06
SNAP23 [NCBI] 1.68728e-06
HNRNPD [NCBI] 1.65702e-06
CUBN [NCBI] 1.64962e-06
CAV1 [NCBI] 1.61565e-06
STC1 [NCBI] 1.57895e-06
GHRL [NCBI] 1.55226e-06
RARA [NCBI] 1.55226e-06
DLG4 [NCBI] 1.54571e-06
DLG1 [NCBI] 1.48903e-06
PRKAR1A [NCBI] 1.45914e-06
STX1A [NCBI] 1.3755e-06
SNAP25 [NCBI] 1.3242e-06
PIH [NCBI] 1.30943e-06
CYP27A1 [NCBI] 1.26672e-06
EPOR [NCBI] 1.06846e-06
CALCA [NCBI] 1.01372e-06
PRKACA [NCBI] 9.6289e-07
KRT20 [NCBI] 9.38795e-07
IAPP [NCBI] 9.01359e-07
PNMT [NCBI] 8.71224e-07
FHIT [NCBI] 8.50135e-07
PRKCE [NCBI] 8.3475e-07
DBH [NCBI] 8.09893e-07
ADM [NCBI] 7.56156e-07
KCNH6 [NCBI] 6.74582e-07
ENG [NCBI] 6.44131e-07
RELA [NCBI] 6.40436e-07
CDKN1B [NCBI] 6.36765e-07
ITGB1 [NCBI] 6.11723e-07
BCL2 [NCBI] 4.9735e-07
HDAC1 [NCBI] 4.95949e-07
NGF [NCBI] 4.41605e-07
CDKN1A [NCBI] 4.36903e-07
NOG [NCBI] 3.81386e-07
PTGS2 [NCBI] 3.79751e-07
VIP [NCBI] 2.60866e-07
TNFRSF11B [NCBI] 2.48798e-07
TNFRSF11A [NCBI] 2.16353e-07
PRKCA [NCBI] 1.97076e-07
BDNF [NCBI] 1.91658e-07
PTGS1 [NCBI] 1.90958e-07
TNFSF11 [NCBI] 1.54113e-07
ACP5 [NCBI] 1.28557e-07
CTSL1 [NCBI] 1.21914e-07
NPY [NCBI] 8.39208e-08
VEGFA [NCBI] 7.19069e-08
BAX [NCBI] 5.61042e-08
PTK2 [NCBI] 4.4597e-08
TH [NCBI] 2.988e-08
PRL [NCBI] 2.88465e-08
TRH [NCBI] 1.40365e-08
NOS2 [NCBI] 8.94669e-09
NOS3 [NCBI] 7.82716e-10



OMIM


 OMIM Link Information
gain		 01
PTH [NCBI] 0.0181248
HHC1 [NCBI] 0.00342309
HYPX [NCBI] 0.00252126
NSHPT [NCBI] 0.00160621
HRPT1 [NCBI] 0.00124284
immune defect due to absence of thymus [NCBI] 0.0011195
CASR [NCBI] 0.000518127
VDR [NCBI] 0.000443071
hyperparathyroidism, primary, caused by water clear cell hyperplasia [NCBI] 0.000386042
velocardiofacial syndrome [NCBI] 0.000346716
PCTT [NCBI] 0.000320594
DGS [NCBI] 0.000243429
EGF [NCBI] 0.000240861
TNF [NCBI] 0.000222565
FIH [NCBI] 0.000205421
hypophosphatemic rickets, x-linked dominant [NCBI] 0.000171513
VEGF [NCBI] 0.000160295
hypercalcemia, idiopathic, of infancy [NCBI] 0.000153522
NGFB [NCBI] 0.000123261
TRS [NCBI] 0.000107588
hypoparathyroidism, sensorineural deafness, and renal disease [NCBI] 0.000104068
PTHLH [NCBI] 9.83694e-05
acromegaly [NCBI] 9.81379e-05
vitamin d-dependent rickets, type i [NCBI] 9.55898e-05
pituitary dwarfism iii [NCBI] 9.32572e-05
BFLS [NCBI] 9.32572e-05
MEN1 [NCBI] 9.30839e-05
HFTC [NCBI] 8.0872e-05
MEN2B [NCBI] 8.0872e-05
NPY [NCBI] 8.00044e-05
SLE [NCBI] 7.15185e-05
FGF23 [NCBI] 7.0416e-05
TH [NCBI] 6.85101e-05
VIP [NCBI] 6.49455e-05
PRL [NCBI] 6.41119e-05
APS1 [NCBI] 5.76744e-05
BDNF [NCBI] 5.70781e-05
CHGA [NCBI] 4.8447e-05
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency [NCBI] 4.2283e-05
TBX1 [NCBI] 3.47751e-05
BGLAP [NCBI] 3.23844e-05
GCM2 [NCBI] 2.98073e-05
hypertension-related calcium-regulated gene [NCBI] 2.98073e-05
PPP2R1B [NCBI] 2.36496e-05
HRPT2 [NCBI] 2.36496e-05
GCM1 [NCBI] 2.18588e-05
FMF [NCBI] 2.12856e-05
RET [NCBI] 1.74276e-05
PTK2 [NCBI] 1.59036e-05
SOX3 [NCBI] 1.52911e-05
FOXE1 [NCBI] 1.47191e-05
KL [NCBI] 1.20678e-05
EGFR [NCBI] 1.14563e-05
FHIT [NCBI] 9.95832e-06
SLC3A2 [NCBI] 9.47219e-06
DLG1 [NCBI] 9.47219e-06
CD [NCBI] 9.13036e-06
PHEX [NCBI] 7.69275e-06
STC1 [NCBI] 3.86041e-06
CCND1 [NCBI] 3.651e-06
GNRH1 [NCBI] 1.86032e-06
ABCB1 [NCBI] 1.67678e-06
PCNA [NCBI] 8.46787e-07
ACP5 [NCBI] 5.36982e-07
ABCC1 [NCBI] 4.18064e-07
PNMT [NCBI] 1.10476e-07
IAPP [NCBI] 1.12976e-08
ADM [NCBI] 5.94843e-10



Database Center for Life Science