Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Hypercalcemia [NCBI]


Gene


Gene Link Information
Gain
01
PTHLH [NCBI] 0.00419928
PTH [NCBI] 0.00254591
CASR [NCBI] 0.00042537
HHC3 [NCBI] 0.000415947
HHC2 [NCBI] 0.000415947
IGAN [NCBI] 8.93865e-05
TNFSF11 [NCBI] 4.63743e-05
TNFRSF11A [NCBI] 4.44542e-05
STC1 [NCBI] 3.19363e-05
VDR [NCBI] 3.15395e-05
MEN1 [NCBI] 2.76014e-05
TNFRSF11B [NCBI] 2.72636e-05
ACP5 [NCBI] 1.78361e-05
ALPL [NCBI] 8.29975e-06
CDC73 [NCBI] 7.68828e-06
FGF23 [NCBI] 7.3815e-06
SLC17A2 [NCBI] 6.59687e-06
SLC34A1 [NCBI] 6.38348e-06
LIF [NCBI] 6.24713e-06
SLC9A3 [NCBI] 5.30794e-06
HLF [NCBI] 4.8928e-06
CALCR [NCBI] 4.28412e-06
CYP27B1 [NCBI] 3.80104e-06
LIMK1 [NCBI] 3.56913e-06
PTH1R [NCBI] 3.21735e-06
PTGS2 [NCBI] 3.08627e-06
TCF3 [NCBI] 3.02954e-06
ELN [NCBI] 2.7334e-06
SLC12A1 [NCBI] 2.63379e-06
ALB [NCBI] 2.61084e-06
PRSS2 [NCBI] 2.43643e-06
CDKN1A [NCBI] 2.36925e-06
PHEX [NCBI] 2.24883e-06
REG1A [NCBI] 1.98457e-06
CFTR [NCBI] 1.89288e-06
SPINK1 [NCBI] 1.82709e-06
CCK [NCBI] 1.77811e-06
CNN1 [NCBI] 1.7159e-06
CYP27A1 [NCBI] 1.7159e-06
RET [NCBI] 1.62482e-06
PRL [NCBI] 1.33381e-06
EGFR [NCBI] 1.30134e-06
AREG [NCBI] 1.23947e-06
AVP [NCBI] 1.19677e-06
EPO [NCBI] 9.47907e-07
GIP [NCBI] 9.41105e-07
MAP2K1 [NCBI] 8.24009e-07
OSM [NCBI] 8.00077e-07
CD99 [NCBI] 7.92256e-07
VIP [NCBI] 6.46911e-07
TNF [NCBI] 4.24858e-07
IL4 [NCBI] 3.64457e-07
EGF [NCBI] 3.34487e-07
CTSL1 [NCBI] 2.74431e-07
AFP [NCBI] 1.05482e-07
TLR4 [NCBI] 2.18388e-08
CALCA [NCBI] 2.44648e-09




OMIM


OMIM Link Information
gain
01
PTH [NCBI] 0.00968709
PTHLH [NCBI] 0.00709551
HHC3 [NCBI] 0.00354984
HHC1 [NCBI] 0.00307973
CASR [NCBI] 0.0013133
HHC2 [NCBI] 0.000938013
WBS [NCBI] 0.000782075
NSHPT [NCBI] 0.00076936
hypercalcemia, idiopathic, of infancy [NCBI] 0.000499178
HRPT1 [NCBI] 0.000434499
SVAS [NCBI] 0.00019449
hypophosphatemic rickets, x-linked dominant [NCBI] 0.000155377
KLK3 [NCBI] 0.000142623
RA [NCBI] 0.000134689
HRPT2 [NCBI] 0.000122833
hyperparathyroidism, neonatal self-limited primary, with hypercalciuria [NCBI] 0.000113012
blue diaper syndrome [NCBI] 9.05549e-05
EGFR [NCBI] 8.86894e-05
PRL [NCBI] 8.47656e-05
TNF [NCBI] 8.24537e-05
parathyroid carcinoma [NCBI] 8.20878e-05
EPO [NCBI] 6.66633e-05
metaphyseal chondrodysplasia, jansen type [NCBI] 6.22404e-05
SLE [NCBI] 6.14777e-05
EGF [NCBI] 6.02806e-05
TNFRSF11B [NCBI] 5.82242e-05
CF [NCBI] 5.46281e-05
VDR [NCBI] 5.24586e-05
AFP [NCBI] 5.0125e-05
STC1 [NCBI] 4.74029e-05
MEN1 [NCBI] 4.63983e-05
alkaptonuria [NCBI] 4.29223e-05
pheochromocytoma [NCBI] 4.08535e-05
hyperoxaluria, primary, type i [NCBI] 3.99157e-05
glycogen storage disease v [NCBI] 3.94676e-05
hypophosphatasia, infantile [NCBI] 3.90323e-05
vitamin d-dependent rickets, type ii [NCBI] 3.90323e-05
AIMAH [NCBI] 3.7407e-05
BGLAP [NCBI] 2.69856e-05
MEN2A [NCBI] 2.54614e-05
APS1 [NCBI] 2.31504e-05
TNFSF11 [NCBI] 2.30309e-05
VHL [NCBI] 2.00218e-05
AREG [NCBI] 1.87286e-05
AVP [NCBI] 1.87047e-05
PTHR1 [NCBI] 1.40422e-05
MUC1 [NCBI] 1.0954e-05
CVID [NCBI] 7.37521e-06
SPP1 [NCBI] 7.06757e-06
VIP [NCBI] 7.02341e-06
ELN [NCBI] 5.99037e-06
CCK [NCBI] 3.84125e-06
RET [NCBI] 1.49039e-06
TLR4 [NCBI] 1.16232e-06
OSM [NCBI] 4.68948e-07
ALB [NCBI] 3.66185e-07
ACP5 [NCBI] 2.53228e-07
GIP [NCBI] 1.02329e-07
TNFSF10 [NCBI] 2.2829e-09




Database Center for Life Science