Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Anemia, Macrocytic [NCBI]

Gene


 Gene Link Information
Gain		 01
TEC [NCBI] 0.000300643
MCEE [NCBI] 1.44579e-05
GIF [NCBI] 1.44579e-05
TMPRSS6 [NCBI] 1.39966e-05
ZFPM1 [NCBI] 1.2756e-05
OPA1 [NCBI] 9.82557e-06
POLG [NCBI] 9.68897e-06
GATA1 [NCBI] 8.4724e-06
SNAI2 [NCBI] 8.2113e-06
RUNX1 [NCBI] 6.9079e-06
HFE [NCBI] 5.42869e-06
HGF [NCBI] 4.97977e-06
EPO [NCBI] 4.42422e-06
CFTR [NCBI] 3.93048e-06



OMIM


 OMIM Link Information
gain		 01
folic acid, transport defect involving [NCBI] 0.00282758
TRMA [NCBI] 0.000714775
CDAN2 [NCBI] 0.000567689
OD [NCBI] 0.000553188
megaloblastic anemia 1 [NCBI] 0.000424895
transcobalamin ii deficiency [NCBI] 0.000323552
homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type [NCBI] 0.000312185
orotic aciduria i [NCBI] 0.000261359
IFD [NCBI] 0.000174719
DBA [NCBI] 0.000162034
anemia, dyserythropoietic congenital, type i [NCBI] 0.000157517
macrocytosis, familial [NCBI] 0.000129339
waardenburg syndrome, type iid [NCBI] 0.000106872
orotic aciduria ii [NCBI] 9.83952e-05
MTR [NCBI] 8.70782e-05
methylcobalamin deficiency, cblg type [NCBI] 7.84898e-05
formiminotransferase deficiency [NCBI] 7.66903e-05
PBT [NCBI] 7.22548e-05
SNAI2 [NCBI] 6.52957e-05
CDAN1 [NCBI] 6.27854e-05
faciogenital dysplasia [NCBI] 5.78898e-05
MTHFD1 [NCBI] 5.76986e-05
pyruvate decarboxylase deficiency [NCBI] 5.22052e-05
WFS1 [NCBI] 5.14874e-05
GATA1 [NCBI] 4.67926e-05
maple syrup urine disease [NCBI] 4.59344e-05
anemia, sideroblastic, x-linked [NCBI] 4.17357e-05
KCNQ1 [NCBI] 3.86021e-05
GPI [NCBI] 2.65926e-05
DHFR [NCBI] 1.66806e-05
HBB [NCBI] 1.48424e-05
CF [NCBI] 7.21974e-06
HGF [NCBI] 7.0448e-06
EPO [NCBI] 4.21476e-06
MG [NCBI] 2.58113e-06
CEACAM5 [NCBI] 1.03925e-06



Database Center for Life Science