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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