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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hypocalcemia [NCBI]

Gene


 Gene Link Information
Gain		 01
PTH [NCBI] 0.00165037
HPT [NCBI] 0.000686903
CASR [NCBI] 0.000220005
TRPM6 [NCBI] 0.000183751
TRPM7 [NCBI] 7.03262e-05
STC1 [NCBI] 6.18171e-05
VDR [NCBI] 4.64747e-05
GATA3 [NCBI] 2.40934e-05
TBX1 [NCBI] 2.13056e-05
FGF23 [NCBI] 1.86549e-05
GCM2 [NCBI] 1.66057e-05
CYP27A1 [NCBI] 1.56027e-05
GNAS [NCBI] 1.39405e-05
CYP27B1 [NCBI] 1.35584e-05
FXYD2 [NCBI] 8.19617e-06
TRPV5 [NCBI] 7.53591e-06
TNFRSF11B [NCBI] 7.48003e-06
PRL [NCBI] 7.19573e-06
PTHLH [NCBI] 6.89685e-06
TBCE [NCBI] 6.86624e-06
TRPV4 [NCBI] 6.53256e-06
HNRNPD [NCBI] 6.45851e-06
BGLAP [NCBI] 6.25406e-06
TRPC6 [NCBI] 6.07177e-06
SOX3 [NCBI] 6.01515e-06
ALB [NCBI] 5.78187e-06
ATP8B1 [NCBI] 5.30101e-06
PTH1R [NCBI] 4.97281e-06
ALPL [NCBI] 4.75044e-06
ACP5 [NCBI] 4.48746e-06
SLC12A3 [NCBI] 4.27967e-06
DBH [NCBI] 3.43838e-06
CALCA [NCBI] 3.04238e-06
IAPP [NCBI] 2.85714e-06
CP [NCBI] 2.57556e-06
EGF [NCBI] 8.48672e-07
TH [NCBI] 4.06223e-07
EGFR [NCBI] 1.51719e-07
EPO [NCBI] 2.26007e-08



OMIM


 OMIM Link Information
gain		 01
PTH [NCBI] 0.00610835
kenny-caffey syndrome, type 2 [NCBI] 0.0048437
CASR [NCBI] 0.00111528
FIH [NCBI] 0.000961413
HOMG [NCBI] 0.000952184
pseudohypoparathyroidism, type ii [NCBI] 0.00092257
HYPX [NCBI] 0.000647644
vitamin d-dependent rickets, type ii [NCBI] 0.000548926
DGS [NCBI] 0.000360228
HOMG3 [NCBI] 0.000342288
AHO [NCBI] 0.000206664
TRPM6 [NCBI] 0.000165538
HRD [NCBI] 0.000153949
VDR [NCBI] 0.000128728
HHC1 [NCBI] 0.000108469
APS1 [NCBI] 7.92342e-05
SLE [NCBI] 7.08578e-05
CYP27B1 [NCBI] 6.83588e-05
TRS [NCBI] 6.82502e-05
osseous heteroplasia, progressive [NCBI] 6.82502e-05
KCS [NCBI] 6.48423e-05
trifunctional protein deficiency [NCBI] 6.33769e-05
BRIC1 [NCBI] 6.20348e-05
NSHPT [NCBI] 6.20348e-05
pituitary dwarfism iii [NCBI] 5.85774e-05
vitamin d-dependent rickets, type i [NCBI] 5.85774e-05
pseudohypoparathyroidism, type ib [NCBI] 5.66302e-05
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency [NCBI] 5.26074e-05
PFIC1 [NCBI] 4.58021e-05
pyruvate decarboxylase deficiency [NCBI] 4.21378e-05
CYP2R1 [NCBI] 4.02842e-05
EGFR [NCBI] 3.42082e-05
GNAS [NCBI] 3.32071e-05
MEN2A [NCBI] 3.10918e-05
wilson disease [NCBI] 2.77215e-05
HADHA [NCBI] 2.63239e-05
SLC12A3 [NCBI] 2.50756e-05
EGF [NCBI] 2.02475e-05
ACP5 [NCBI] 2.02292e-05
CSF2 [NCBI] 2.01981e-05
PDHA1 [NCBI] 1.83459e-05
EPO [NCBI] 1.75544e-05
polycystic kidneys [NCBI] 1.03935e-05
ALB [NCBI] 8.17854e-06
BGLAP [NCBI] 7.08677e-06
TH [NCBI] 5.05745e-06
IAPP [NCBI] 4.60038e-06
CP [NCBI] 2.93438e-06
TNFRSF11B [NCBI] 2.6513e-06
SPP1 [NCBI] 8.44655e-08
PTHLH [NCBI] 2.38184e-08
PRL [NCBI] 4.25799e-13



Database Center for Life Science