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MeSH keywords -> Related genes, diseases (OMIM)


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01 Anemia, Hypochromic [NCBI]


Gene


Gene Link Information
Gain
01
TEC [NCBI] 0.000300643
EPO [NCBI] 0.000210094
HBA1 [NCBI] 6.61081e-05
HBA2 [NCBI] 6.06031e-05
TF [NCBI] 4.27354e-05
DMRT1 [NCBI] 3.17197e-05
SLC11A1 [NCBI] 1.91566e-05
HFE [NCBI] 1.81898e-05
CYBRD1 [NCBI] 9.76214e-06
SLC11A2 [NCBI] 9.64773e-06
HEPH [NCBI] 9.34426e-06
OXCT2 [NCBI] 8.00188e-06
FECH [NCBI] 7.6244e-06
HBG2 [NCBI] 7.49409e-06
HAMP [NCBI] 7.40252e-06
HBD [NCBI] 7.05442e-06
EPOR [NCBI] 6.07222e-06
EPB41L1 [NCBI] 6.0321e-06
MB [NCBI] 5.99291e-06
EPB41L2 [NCBI] 5.85658e-06
TFRC [NCBI] 5.13377e-06
CP [NCBI] 4.94454e-06
MPL [NCBI] 4.91051e-06
MPO [NCBI] 4.80307e-06
HP [NCBI] 4.28567e-06
TTR [NCBI] 3.65961e-06
LIF [NCBI] 3.2798e-06
ADA [NCBI] 2.94455e-06
G6PD [NCBI] 2.85252e-06
ACHE [NCBI] 2.25028e-06
EGF [NCBI] 6.10966e-07
TNF [NCBI] 8.18769e-08




OMIM


OMIM Link Information
gain
01
koilonychia, hereditary [NCBI] 0.00200072
enteropathy, protein-losing [NCBI] 0.00119841
GHDD [NCBI] 0.000844965
kenny-caffey syndrome, type 2 [NCBI] 0.000672238
EPO [NCBI] 0.00066805
atransferrinemia [NCBI] 0.000402934
anemia, sideroblastic, x-linked [NCBI] 0.000401501
anemia, hypochromic microcytic [NCBI] 0.000322163
anemia, microcytic [NCBI] 0.000309301
HBA1 [NCBI] 0.000295179
beeturia [NCBI] 0.00025071
HBA2 [NCBI] 0.000233109
HBB [NCBI] 0.000144019
TF [NCBI] 0.000141805
hyperzincemia with functional zinc depletion [NCBI] 0.000125147
neutrophilia, hereditary [NCBI] 0.000125147
hemosiderosis, pulmonary, with deficiency of gamma-a globulin [NCBI] 0.000125147
SLC11A2 [NCBI] 0.00011918
HEPH [NCBI] 9.45178e-05
pernicious anemia [NCBI] 8.46164e-05
chromosome 5q deletion syndrome [NCBI] 6.68414e-05
erythrocytosis, familial, 1 [NCBI] 6.46153e-05
aceruloplasminemia [NCBI] 6.46153e-05
JLNS1 [NCBI] 6.09211e-05
OPTB3 [NCBI] 6.01173e-05
glycogen storage disease ib [NCBI] 5.42804e-05
NFE2 [NCBI] 5.17019e-05
PDXK [NCBI] 4.9196e-05
PCTT [NCBI] 4.80838e-05
XG [NCBI] 4.2882e-05
RA [NCBI] 4.12243e-05
CA2 [NCBI] 4.0791e-05
SLE [NCBI] 3.95426e-05
CP [NCBI] 3.57851e-05
HAMP [NCBI] 3.57509e-05
CD [NCBI] 3.43952e-05
TFRC [NCBI] 3.13146e-05
HBD [NCBI] 2.85517e-05
EPOR [NCBI] 2.00465e-05
thrombocytopenic purpura, autoimmune [NCBI] 1.8972e-05
MB [NCBI] 1.70862e-05
apc gene [NCBI] 1.51254e-05
HFE [NCBI] 1.23035e-05
HP [NCBI] 8.77017e-06
EGF [NCBI] 5.95243e-06
CEACAM5 [NCBI] 5.19533e-06
TTR [NCBI] 4.1872e-06
APC [NCBI] 2.82089e-06
ADA [NCBI] 2.193e-06
MPO [NCBI] 1.50803e-06
G6PD [NCBI] 1.21043e-06
ACHE [NCBI] 3.66028e-07




Database Center for Life Science