Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Anemia, Megaloblastic	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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