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MeSH keywords -> Related genes, diseases (OMIM)


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01 Erythrocyte Aging [NCBI]


Gene


Gene Link Information
Gain
01
EPB41L1 [NCBI] 5.31542e-05
EPB41L2 [NCBI] 5.24285e-05
G6PD [NCBI] 2.22905e-05
ACHE [NCBI] 1.95067e-05
EPO [NCBI] 1.32287e-05
SPTB [NCBI] 5.6439e-06
SPTA1 [NCBI] 5.31462e-06
TF [NCBI] 5.28239e-06
CD59 [NCBI] 4.81429e-06
PTH [NCBI] 4.6126e-06
OLR1 [NCBI] 4.46172e-06
HBA1 [NCBI] 4.23621e-06
HBQ1 [NCBI] 3.30292e-06
SLC12A4 [NCBI] 3.14296e-06
STAB2 [NCBI] 2.97566e-06
UCK2 [NCBI] 2.95291e-06
ANXA7 [NCBI] 2.91057e-06
PFKL [NCBI] 2.89079e-06
HBZ [NCBI] 2.89079e-06
DPP3 [NCBI] 2.87184e-06
AK1 [NCBI] 2.77222e-06
ITPA [NCBI] 2.75756e-06
CLNS1A [NCBI] 2.7032e-06
LIMS1 [NCBI] 2.60049e-06
HK1 [NCBI] 2.56137e-06
CAST [NCBI] 2.40451e-06
HBE1 [NCBI] 2.40451e-06
SIRPA [NCBI] 2.32006e-06
HBD [NCBI] 2.24423e-06
CD55 [NCBI] 2.23502e-06
CR1 [NCBI] 2.23048e-06
DARC [NCBI] 2.19573e-06
HBG1 [NCBI] 2.15573e-06
KLF1 [NCBI] 2.15192e-06
PTPN1 [NCBI] 2.11899e-06
AQP1 [NCBI] 2.10853e-06
HBA2 [NCBI] 2.0753e-06
CD47 [NCBI] 1.97516e-06
SLC4A1 [NCBI] 1.95755e-06
ACTB [NCBI] 1.95755e-06
FCGR3A [NCBI] 1.90191e-06
EPOR [NCBI] 1.76244e-06
SCARB1 [NCBI] 1.75295e-06
CASP8 [NCBI] 1.7227e-06
BCHE [NCBI] 1.68755e-06
HBB [NCBI] 1.59618e-06
BAK1 [NCBI] 1.54523e-06
FADD [NCBI] 1.49777e-06
FAS [NCBI] 1.36732e-06
FOLR1 [NCBI] 1.33081e-06
BCL2L1 [NCBI] 9.01862e-07
CAT [NCBI] 8.98796e-07
FASLG [NCBI] 7.02082e-07
CASP3 [NCBI] 4.66187e-07
TNF [NCBI] 2.35347e-07




OMIM


OMIM Link Information
gain
01
DHS [NCBI] 0.00272141
stomatocytosis i [NCBI] 0.00162635
CDAN3 [NCBI] 0.000865622
hexokinase deficiency hemolytic anemia [NCBI] 0.00050843
gilbert syndrome [NCBI] 0.000322775
G6PD [NCBI] 0.000265607
RHN [NCBI] 0.000219187
woronets trait [NCBI] 0.000156965
pyruvate kinase deficiency of red cells [NCBI] 0.000154837
magnesium, elevated red cell [NCBI] 0.000129199
gastritis, familial giant hypertrophic [NCBI] 0.000111924
SLC4A1 [NCBI] 9.8287e-05
crigler-najjar syndrome, type ii [NCBI] 9.41293e-05
ACHE [NCBI] 9.21682e-05
uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to [NCBI] 8.99073e-05
phosphoglycerate kinase 1 deficiency [NCBI] 8.99073e-05
SPTB [NCBI] 8.54522e-05
anemia, dyserythropoietic congenital, type i [NCBI] 8.48927e-05
TTP [NCBI] 8.21394e-05
porphyria, congenital erythropoietic [NCBI] 7.75699e-05
CHAC [NCBI] 7.56289e-05
HS [NCBI] 7.49296e-05
glycogen storage disease vii [NCBI] 6.74356e-05
malaria, susceptibility to [NCBI] 6.56899e-05
porphyria, acute intermittent [NCBI] 6.21386e-05
EPO [NCBI] 5.86161e-05
CMPK1 [NCBI] 5.82136e-05
HBB [NCBI] 4.12774e-05
GUK3 [NCBI] 3.94863e-05
thrombocytopenic purpura, autoimmune [NCBI] 3.93745e-05
CLNS1A [NCBI] 3.43555e-05
LIMS1 [NCBI] 3.43555e-05
PDXK [NCBI] 2.98131e-05
PRDX2 [NCBI] 2.90694e-05
Ss [NCBI] 2.84089e-05
TF [NCBI] 2.7643e-05
ITPA [NCBI] 2.72752e-05
CAST [NCBI] 2.47879e-05
JMJD6 [NCBI] 2.47879e-05
GPI [NCBI] 2.42946e-05
LCAT [NCBI] 2.32462e-05
HK1 [NCBI] 2.25632e-05
GPX1 [NCBI] 2.19072e-05
GSTP1 [NCBI] 2.15075e-05
AK1 [NCBI] 2.11335e-05
MN [NCBI] 2.09551e-05
RHCE [NCBI] 1.98397e-05
FY [NCBI] 1.96965e-05
methemoglobinemia due to deficiency of methemoglobin reductase [NCBI] 1.87827e-05
CD47 [NCBI] 1.86632e-05
RA [NCBI] 1.69242e-05
HBA2 [NCBI] 1.29663e-05
EPOR [NCBI] 1.06337e-05
CF [NCBI] 9.59547e-06
PTH [NCBI] 8.49628e-06
BCHE [NCBI] 8.21079e-06
TNF [NCBI] 5.74064e-06
CAT [NCBI] 5.4325e-07
AD [NCBI] 2.5549e-07




Database Center for Life Science