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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hematuria [NCBI]


Gene


Gene Link Information
Gain
01
IGAN [NCBI] 0.0103478
COL4A4 [NCBI] 0.000228456
COL4A3 [NCBI] 0.000134049
KTWS [NCBI] 0.000109959
COL4A5 [NCBI] 8.15817e-05
UMOD [NCBI] 4.22232e-05
AMBP [NCBI] 3.71978e-05
COL4A1 [NCBI] 1.92583e-05
BIRC5 [NCBI] 1.21689e-05
TNFAIP1 [NCBI] 1.07029e-05
MGEA5 [NCBI] 1.07029e-05
PKD1 [NCBI] 1.01868e-05
COL4A2 [NCBI] 9.36807e-06
TRPM8 [NCBI] 8.20364e-06
NPHS2 [NCBI] 7.61462e-06
SLC22A12 [NCBI] 7.48675e-06
PODXL [NCBI] 7.10251e-06
FGA [NCBI] 6.83074e-06
MYH9 [NCBI] 6.70963e-06
IL1R1 [NCBI] 6.69026e-06
FN1 [NCBI] 6.49068e-06
CD68 [NCBI] 6.46317e-06
IL1RN [NCBI] 6.12006e-06
MYOD1 [NCBI] 6.01649e-06
RAG2 [NCBI] 5.89209e-06
WT1 [NCBI] 5.57615e-06
SERPINA1 [NCBI] 5.24428e-06
VWF [NCBI] 5.04795e-06
NPHS1 [NCBI] 4.82313e-06
IGFBP3 [NCBI] 4.78577e-06
SCGB1A1 [NCBI] 4.72533e-06
CD99 [NCBI] 4.62188e-06
PCNA [NCBI] 4.4101e-06
KRT7 [NCBI] 4.20648e-06
IL2 [NCBI] 4.13485e-06
F8 [NCBI] 4.0584e-06
HMOX1 [NCBI] 3.93739e-06
FGFR3 [NCBI] 3.81482e-06
FHIT [NCBI] 3.6517e-06
IL1B [NCBI] 3.07534e-06
HLA-DRB1 [NCBI] 2.51048e-06
IL6 [NCBI] 2.25374e-06
NOS2 [NCBI] 1.94881e-06
TGFB1 [NCBI] 1.56959e-06
AR [NCBI] 1.48551e-06
TNF [NCBI] 1.35059e-06
CFTR [NCBI] 1.02261e-06
PTH [NCBI] 7.21465e-07




OMIM


OMIM Link Information
gain
01
alport syndrome, autosomal dominant [NCBI] 0.00708016
renal failure, progressive, with hypertension [NCBI] 0.00452734
IGAN1 [NCBI] 0.00278078
BFH [NCBI] 0.00106474
klippel-trenaunay-weber syndrome [NCBI] 0.000922599
ATS [NCBI] 0.000253024
alport syndrome, autosomal recessive [NCBI] 0.000241564
HANAC [NCBI] 0.000188729
COL4A4 [NCBI] 0.000128409
cryofibrinogenemia, familial primary [NCBI] 0.000116703
thrombocytopenia with elevated serum iga and renal disease [NCBI] 0.000116703
polycystic kidneys [NCBI] 0.000112204
SLE [NCBI] 0.000104541
COL4A3 [NCBI] 0.000100817
beeturia [NCBI] 9.42421e-05
hypervitaminosis a, susceptibility to [NCBI] 9.42421e-05
deafness, cochlear, with myopia and intellectual impairment [NCBI] 9.42421e-05
factor viii deficiency [NCBI] 8.57719e-05
coloboma, uveal, with cleft lip and palate and mental retardation [NCBI] 8.57719e-05
fibrosclerosis, multifocal [NCBI] 8.02756e-05
membranoproliferative glomerulonephritis, x-linked [NCBI] 7.61917e-05
charcot-marie-tooth disease and deafness [NCBI] 7.29396e-05
donnai-barrow syndrome [NCBI] 7.02373e-05
hyperprolinemia, type i [NCBI] 5.96972e-05
COL4A1 [NCBI] 5.51571e-05
methylmalonic aciduria and homocystinuria, cblc type [NCBI] 5.02861e-05
NPHS1 [NCBI] 4.95931e-05
COL4A5 [NCBI] 4.21681e-05
C3 [NCBI] 4.12686e-05
HBB [NCBI] 4.0503e-05
UGB [NCBI] 3.8979e-05
factor x deficiency [NCBI] 3.8979e-05
HAE [NCBI] 3.4966e-05
FGA [NCBI] 3.46508e-05
RNASE3 [NCBI] 3.41471e-05
HPRT1 [NCBI] 3.04608e-05
wilson disease [NCBI] 2.55448e-05
CEACAM5 [NCBI] 2.16934e-05
KLK3 [NCBI] 2.14857e-05
PCNA [NCBI] 1.46025e-05
WAS [NCBI] 1.14102e-05
temporal arteritis [NCBI] 6.53826e-06
AR [NCBI] 4.89922e-06
FMF [NCBI] 3.62109e-06
RA [NCBI] 2.30465e-06
PTH [NCBI] 7.55162e-07
VEGF [NCBI] 4.4709e-07
TNF [NCBI] 1.47454e-07
thrombocytopenic purpura, autoimmune [NCBI] 6.35105e-08




Database Center for Life Science