MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Hypoparathyroidism
[NCBI]
Gene
Gene
Link
Information
Gain
01
HPT
[NCBI]
0.00428266
PTH
[NCBI]
0.000993428
GATA3
[NCBI]
0.00018131
GCM2
[NCBI]
0.000154032
PKC
[NCBI]
0.000140853
CASR
[NCBI]
0.000128098
TBCE
[NCBI]
0.000106105
SOX3
[NCBI]
4.78919e-05
FGF23
[NCBI]
3.62165e-05
GNAS
[NCBI]
3.09928e-05
PTHLH
[NCBI]
3.02855e-05
TBX1
[NCBI]
2.33471e-05
TBCA
[NCBI]
1.42632e-05
ATP11A
[NCBI]
1.42632e-05
CDC73
[NCBI]
1.25948e-05
NLRP5
[NCBI]
1.18831e-05
AIRE
[NCBI]
1.18102e-05
ATP11C
[NCBI]
1.0985e-05
CYP27A1
[NCBI]
1.03579e-05
SOX1
[NCBI]
8.51319e-06
TRPV5
[NCBI]
8.21445e-06
HIRA
[NCBI]
7.63856e-06
MCF2
[NCBI]
7.13477e-06
TPO
[NCBI]
7.064e-06
TRPM6
[NCBI]
6.8056e-06
RET
[NCBI]
5.81203e-06
PTH1R
[NCBI]
5.64226e-06
PHEX
[NCBI]
4.60659e-06
VDR
[NCBI]
4.20237e-06
PRL
[NCBI]
3.84122e-06
PTPN22
[NCBI]
3.55287e-06
CTLA4
[NCBI]
2.67348e-06
MEN1
[NCBI]
2.44034e-06
ACP5
[NCBI]
1.797e-06
TNFRSF11A
[NCBI]
1.68017e-06
TNFSF11
[NCBI]
1.48159e-06
CALCA
[NCBI]
1.11715e-06
TRH
[NCBI]
1.07621e-06
EPO
[NCBI]
2.2782e-07
OMIM
OMIM
Link
Information
gain
01
HYPX
[NCBI]
0.00716102
PTH
[NCBI]
0.00367845
kenny-caffey syndrome, type 2
[NCBI]
0.00353711
FIH
[NCBI]
0.00307631
digeorge syndrome/velocardiofacial syndrome spectrum of malformation 2
[NCBI]
0.00198466
APS1
[NCBI]
0.00186523
hypoparathyroidism, sensorineural deafness, and renal disease
[NCBI]
0.00104992
HRD
[NCBI]
0.00104992
IBGC1
[NCBI]
0.000824049
pseudohypoparathyroidism, type ii
[NCBI]
0.000714117
CASR
[NCBI]
0.000666068
megalencephaly
[NCBI]
0.000632262
DGS
[NCBI]
0.000545258
EKD1
[NCBI]
0.000486102
APS2
[NCBI]
0.000395025
IGAD1
[NCBI]
0.000300739
dubowitz syndrome
[NCBI]
0.000287577
GATA3
[NCBI]
0.000256779
KCS
[NCBI]
0.000225205
TBCE
[NCBI]
0.000222568
RA
[NCBI]
0.000222339
GCM2
[NCBI]
0.000180101
AHO
[NCBI]
0.0001692
HHC1
[NCBI]
0.000155061
SLE
[NCBI]
0.000155027
AIRE
[NCBI]
0.000111079
lymphedema-hypoparathyroidism syndrome
[NCBI]
0.000109689
KSS
[NCBI]
9.29171e-05
macrocephaly
[NCBI]
7.87713e-05
ATP11C
[NCBI]
6.74226e-05
ATP11B
[NCBI]
6.74226e-05
ATP11A
[NCBI]
6.74226e-05
TRS
[NCBI]
5.89447e-05
HHS
[NCBI]
5.55532e-05
trifunctional protein deficiency
[NCBI]
5.4096e-05
NSHPT
[NCBI]
5.27622e-05
pituitary dwarfism iii
[NCBI]
4.93294e-05
autoimmune disease
[NCBI]
4.83341e-05
PNKD1
[NCBI]
3.7641e-05
SOX3
[NCBI]
3.63038e-05
cystinuria
[NCBI]
3.5006e-05
BGLAP
[NCBI]
3.46468e-05
SLC7A9
[NCBI]
3.25119e-05
CD
[NCBI]
3.00824e-05
wilson disease
[NCBI]
1.92534e-05
GNAS
[NCBI]
1.46475e-05
VDR
[NCBI]
5.04967e-06
TPO
[NCBI]
4.25155e-06
PTHLH
[NCBI]
1.28985e-06
panencephalitis, subacute sclerosing
[NCBI]
7.79734e-07
PRL
[NCBI]
1.03021e-08
Database Center for Life Science