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MeSH keywords -> Related genes, diseases (OMIM)


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01 Nephrocalcinosis [NCBI]

Gene


 Gene Link Information
Gain		 01
CLCN5 [NCBI] 0.000107578
CLDN16 [NCBI] 9.50867e-05
PTH [NCBI] 3.21421e-05
ATP6V1B1 [NCBI] 2.42373e-05
CA2 [NCBI] 2.07381e-05
ND4L [NCBI] 1.70269e-05
UMOD [NCBI] 1.20898e-05
KCNJ1 [NCBI] 9.23222e-06
SLC26A3 [NCBI] 9.18323e-06
CLCNKB [NCBI] 8.64848e-06
OCRL [NCBI] 8.41756e-06
ALPL [NCBI] 8.16024e-06
SLC4A1 [NCBI] 7.71849e-06
CLCN1 [NCBI] 7.67801e-06
PHEX [NCBI] 7.33501e-06
AGXT2L1 [NCBI] 7.16407e-06
SPINT2 [NCBI] 7.07761e-06
REG1A [NCBI] 7.03598e-06
CASR [NCBI] 6.53013e-06
FGF23 [NCBI] 5.69087e-06
CFTR [NCBI] 5.68956e-06
AMBP [NCBI] 5.56605e-06
OSM [NCBI] 5.54895e-06
LIF [NCBI] 4.19548e-06
VDR [NCBI] 3.54405e-06



OMIM


 OMIM Link Information
gain		 01
alport syndrome, autosomal dominant [NCBI] 0.000841397
CLCN5 [NCBI] 0.000552618
hyperoxaluria, primary, type i [NCBI] 0.000387376
CLDN16 [NCBI] 0.000373481
proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis [NCBI] 0.000371344
HOMG3 [NCBI] 0.000359402
renal tubular acidosis, distal, autosomal dominant [NCBI] 0.000349341
dent disease 1 [NCBI] 0.000245692
AI1G [NCBI] 0.000215851
hypomagnesemia, renal, with ocular involvement [NCBI] 0.000215851
hypophosphatemic rickets, x-linked dominant [NCBI] 0.000186169
XRN [NCBI] 0.000178949
xanthinuria, type ii [NCBI] 0.000123215
FIH [NCBI] 0.000120946
blue diaper syndrome [NCBI] 0.00010075
PTH [NCBI] 9.66959e-05
renal tubular acidosis, proximal [NCBI] 9.22761e-05
RTADR [NCBI] 8.26879e-05
hypophosphatemic rickets, x-linked recessive [NCBI] 8.26879e-05
glycogen storage disease i [NCBI] 8.26378e-05
hyperoxaluria, primary, type ii [NCBI] 7.94318e-05
renal tubular acidosis, proximal, with ocular abnormalities and mental retardation [NCBI] 7.67254e-05
CASR [NCBI] 6.81382e-05
renal tubular acidosis, distal, with progressive nerve deafness [NCBI] 6.61613e-05
xanthinuria, type i [NCBI] 6.26967e-05
bartter syndrome, antenatal, type 2 [NCBI] 6.26967e-05
SLC18A3 [NCBI] 3.94339e-05
fructose intolerance, hereditary [NCBI] 3.86109e-05
SLC4A1 [NCBI] 3.4232e-05
cortisol 11-beta-ketoreductase deficiency [NCBI] 3.26831e-05
wilson disease [NCBI] 3.16156e-05
MAS [NCBI] 3.02915e-05
SLE [NCBI] 2.5356e-05
OSM [NCBI] 2.41651e-05
WBS [NCBI] 2.28265e-05
PJS [NCBI] 2.1365e-05
BWS [NCBI] 1.62991e-05
PTHLH [NCBI] 1.37019e-05
VDR [NCBI] 9.85074e-06
CF [NCBI] 1.55816e-06



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