Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Anemia, Megaloblastic [NCBI]

Gene


 Gene Link Information
Gain		 01
SLC19A2 [NCBI] 0.000263921
CUBN [NCBI] 0.000139715
AMN [NCBI] 7.54517e-05
GIF [NCBI] 2.65096e-05
MTRR [NCBI] 2.52317e-05
TCN2 [NCBI] 2.14603e-05
TPK1 [NCBI] 1.25356e-05
MCEE [NCBI] 1.19024e-05
SLC19A3 [NCBI] 1.12502e-05
FOLR1 [NCBI] 4.77571e-06
HRAS [NCBI] 3.12425e-06
MBP [NCBI] 2.58192e-06
CDKN1A [NCBI] 1.44605e-06
EGF [NCBI] 1.14272e-06



OMIM


 OMIM Link Information
gain		 01
folic acid, transport defect involving [NCBI] 0.0030029
TRMA [NCBI] 0.00173296
megaloblastic anemia 1 [NCBI] 0.00152297
methylmalonic aciduria and homocystinuria, cbld type [NCBI] 0.000844965
SLC19A2 [NCBI] 0.000843849
homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type [NCBI] 0.000698461
CUBN [NCBI] 0.000497938
transcobalamin ii deficiency [NCBI] 0.000446652
methylcobalamin deficiency, cblg type [NCBI] 0.000394917
AMN [NCBI] 0.000295629
IFD [NCBI] 0.000162322
MTR [NCBI] 0.000129022
intrinsic factor and r binder, combined congenital deficiency of [NCBI] 0.000123215
cystic fibrosis with helicobacter pylori gastritis, megaloblastic anemia, and subnormal mentality [NCBI] 0.000123215
MTRR [NCBI] 0.000121485
TPK1 [NCBI] 8.29498e-05
GIF [NCBI] 6.05968e-05
pyruvate decarboxylase deficiency [NCBI] 4.61907e-05
WFS1 [NCBI] 4.54781e-05
maple syrup urine disease [NCBI] 3.99736e-05
MTHFR [NCBI] 3.14398e-05
IFNA1 [NCBI] 2.5036e-05
DHFR [NCBI] 1.24233e-05
MBP [NCBI] 3.49106e-06
MG [NCBI] 4.48731e-07
EGF [NCBI] 4.59306e-09
CEACAM5 [NCBI] 2.36782e-09



Database Center for Life Science