Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Calcium Metabolism Disorders [NCBI]

Gene


 Gene Link Information
Gain		 01
HCA1 [NCBI] 0.000438875
PTH [NCBI] 0.000173093
CASR [NCBI] 7.04679e-05
VDR [NCBI] 3.18629e-05
TRPV5 [NCBI] 2.45975e-05
FGF23 [NCBI] 1.38711e-05
WNK4 [NCBI] 8.72597e-06
ITPR1 [NCBI] 7.06396e-06
CYP27A1 [NCBI] 6.76543e-06
ENPP1 [NCBI] 6.64441e-06
PTHLH [NCBI] 3.78035e-06



OMIM


 OMIM Link Information
gain		 01
hypercalciuria, absorptive, 1 [NCBI] 0.00137383
PTH [NCBI] 0.000664376
HCA2 [NCBI] 0.000467851
CASR [NCBI] 0.000266575
VDR [NCBI] 0.000119893
hypomagnesemia, renal, with ocular involvement [NCBI] 0.000109365
AI1G [NCBI] 0.000109365
RTADR [NCBI] 9.97657e-05
hypophosphatemic rickets, x-linked recessive [NCBI] 9.97657e-05
XRN [NCBI] 9.37927e-05
HHRH [NCBI] 8.60195e-05
proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis [NCBI] 8.45465e-05
pulmonary alveolar microlithiasis [NCBI] 8.19513e-05
xanthinuria, type i [NCBI] 7.97164e-05
dent disease 1 [NCBI] 7.97164e-05
OPTB1 [NCBI] 7.0453e-05
CCAL2 [NCBI] 6.93203e-05
hyperoxaluria, primary, type i [NCBI] 6.67957e-05
WNK4 [NCBI] 4.90509e-05
PXE [NCBI] 3.66106e-05
BWS [NCBI] 3.17359e-05
AVP [NCBI] 3.05464e-06
CF [NCBI] 1.63509e-07



Database Center for Life Science