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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hypophosphatemia, Familial [NCBI]

Gene


 Gene Link Information
Gain		 01
PHEX [NCBI] 0.000559251
FGF23 [NCBI] 0.000523255
VDR [NCBI] 0.000157727
MEPE [NCBI] 7.7329e-05
PTH [NCBI] 7.29385e-05
SLC17A2 [NCBI] 5.00414e-05
SLC34A1 [NCBI] 3.48185e-05
CLCN5 [NCBI] 1.71479e-05
DYRK4 [NCBI] 1.48727e-05
C12orf4 [NCBI] 1.48727e-05
LPAR5 [NCBI] 1.24925e-05
SLC17A1 [NCBI] 1.24925e-05
GALNT8 [NCBI] 1.24925e-05
CYP27A1 [NCBI] 1.15618e-05
C12orf5 [NCBI] 1.10111e-05
IBSP [NCBI] 1.05997e-05
SLC34A2 [NCBI] 1.0232e-05
SLC34A3 [NCBI] 9.94481e-06
NT5C3 [NCBI] 8.96541e-06
STC2 [NCBI] 8.82245e-06
GALNT3 [NCBI] 8.56806e-06
CYP24A1 [NCBI] 7.97505e-06
SFRP4 [NCBI] 7.13546e-06
STC1 [NCBI] 6.65111e-06
DSPP [NCBI] 6.53997e-06
OCRL [NCBI] 6.27505e-06
ALPL [NCBI] 6.01965e-06
SFRP1 [NCBI] 5.8448e-06
RELB [NCBI] 5.77511e-06
AMH [NCBI] 4.71724e-06
FAH [NCBI] 4.63524e-06
ENPP1 [NCBI] 4.48267e-06
SAT2 [NCBI] 4.2415e-06
FGF7 [NCBI] 3.90349e-06
FGFR3 [NCBI] 2.66863e-06
ACP5 [NCBI] 2.32956e-06
ADA [NCBI] 1.87125e-06
AVP [NCBI] 1.21696e-06



OMIM


 OMIM Link Information
gain		 01
HBD [NCBI] 0.00621733
hypophosphatemic rickets, x-linked dominant [NCBI] 0.00488058
vitamin d-dependent rickets, type ii [NCBI] 0.00183408
PHEX [NCBI] 0.00150299
ADHR [NCBI] 0.000785723
VDR [NCBI] 0.000781774
vitamin d-dependent rickets, type ii, with normal vitamin d receptor [NCBI] 0.000765046
HHC3 [NCBI] 0.000711792
dentin dysplasia, type i [NCBI] 0.000672238
HHRH [NCBI] 0.000543788
fanconi renotubular syndrome [NCBI] 0.000539786
diarrhea 2, with microvillous atrophy [NCBI] 0.000539786
FGF23 [NCBI] 0.00049378
vitamin d-dependent rickets, type i [NCBI] 0.000394132
hypophosphatemic rickets, autosomal recessive [NCBI] 0.000277993
PTH [NCBI] 0.000225157
hypophosphatemic rickets, x-linked recessive [NCBI] 0.000167005
SLC34A1 [NCBI] 0.000114077
hypophosphatemia, renal, with intracerebral calcifications [NCBI] 0.000110667
HFTC [NCBI] 0.000101791
GALNT3 [NCBI] 0.00010016
CLCN5 [NCBI] 8.2985e-05
nevus, keratinocytic, nonepidermolytic [NCBI] 7.97469e-05
GPR92 [NCBI] 7.36979e-05
GALNT8 [NCBI] 7.36979e-05
GLRA2 [NCBI] 5.99231e-05
HCA2 [NCBI] 5.99137e-05
MAS [NCBI] 5.83995e-05
dentinogenesis imperfecta, shields type iii [NCBI] 5.81263e-05
liddle syndrome [NCBI] 5.50618e-05
HOMG3 [NCBI] 5.24962e-05
SLC34A3 [NCBI] 5.13558e-05
paget disease, juvenile [NCBI] 5.02908e-05
dent disease 1 [NCBI] 5.02908e-05
DGI1 [NCBI] 5.02908e-05
SMS [NCBI] 4.885e-05
KFSD [NCBI] 4.74743e-05
GACI [NCBI] 4.43705e-05
bartter syndrome, type 3 [NCBI] 3.90729e-05
hypophosphatasia, infantile [NCBI] 3.6772e-05
DSPP [NCBI] 3.21039e-05
CLS [NCBI] 2.80323e-05
RS1 [NCBI] 2.76939e-05
SPP1 [NCBI] 1.73905e-05
AMH [NCBI] 1.51155e-05
ACP5 [NCBI] 6.84307e-06
ADA [NCBI] 2.01341e-06
AVP [NCBI] 1.77169e-08



Database Center for Life Science