Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Glycosuria [NCBI]

Gene


 Gene Link Information
Gain		 01
GLYS1 [NCBI] 0.000499621
SLC5A2 [NCBI] 2.5968e-05
HNF1A [NCBI] 2.40744e-05
AMBP [NCBI] 1.55101e-05
HNF1B [NCBI] 1.4877e-05
INS [NCBI] 1.46897e-05
AGA [NCBI] 9.84985e-06
OCRL [NCBI] 9.39216e-06
IL15 [NCBI] 8.93412e-06
TNFRSF9 [NCBI] 8.86463e-06
PHEX [NCBI] 8.30782e-06
SPINT2 [NCBI] 8.04979e-06
REG1A [NCBI] 8.00805e-06
HBB [NCBI] 6.84779e-06
FGF23 [NCBI] 6.65742e-06
CAV1 [NCBI] 6.6389e-06
SCGB1A1 [NCBI] 6.60847e-06
RAG1 [NCBI] 6.05762e-06
UMOD [NCBI] 5.81124e-06
CDK4 [NCBI] 5.18064e-06
CST3 [NCBI] 4.83176e-06
NOS3 [NCBI] 3.91205e-06
PCNA [NCBI] 2.84698e-06
PTH [NCBI] 2.24116e-06



OMIM


 OMIM Link Information
gain		 01
MRSD [NCBI] 0.00107364
fanconi renotubular syndrome [NCBI] 0.000765046
diabetes mellitus, transient neonatal, 1 [NCBI] 0.000645584
GLYS1 [NCBI] 0.000584448
GGM [NCBI] 0.000194697
glucoglycinuria [NCBI] 0.000137445
sucrosuria, hiatus hernia and mental retardation [NCBI] 0.000114976
fructose intolerance, hereditary [NCBI] 0.000107464
MODY [NCBI] 9.23832e-05
renal cysts and diabetes syndrome [NCBI] 8.03344e-05
galactokinase deficiency [NCBI] 7.58451e-05
INS [NCBI] 7.33698e-05
FBS [NCBI] 7.31462e-05
hartnup disorder [NCBI] 7.31462e-05
NPHP1 [NCBI] 6.64672e-05
OCRL [NCBI] 6.44189e-05
hypophosphatemic rickets, x-linked dominant [NCBI] 5.7821e-05
CTNS [NCBI] 5.68953e-05
HNF1B [NCBI] 5.1408e-05
aspartylglucosaminuria [NCBI] 4.83906e-05
SLC2A2 [NCBI] 4.66106e-05
UGB [NCBI] 4.48727e-05
tyrosinemia, type i [NCBI] 4.06738e-05
CDK4 [NCBI] 3.54884e-05
AGER [NCBI] 3.4029e-05
PPARA [NCBI] 1.99584e-05
RA [NCBI] 1.6479e-05
PCNA [NCBI] 6.40197e-06
PTH [NCBI] 3.73935e-06



Database Center for Life Science