MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Homocystinuria
[NCBI]
Gene
Gene
Link
Information
Gain
01
CBS
[NCBI]
0.000577446
MMACHC
[NCBI]
0.000135889
MTRR
[NCBI]
6.36097e-05
FBN1
[NCBI]
2.3866e-05
MTR
[NCBI]
2.25344e-05
MTHFR
[NCBI]
1.76594e-05
C2orf25
[NCBI]
1.59993e-05
CBLC
[NCBI]
1.10705e-05
MAT1A
[NCBI]
1.00904e-05
NAGS
[NCBI]
8.72467e-06
CST3
[NCBI]
8.10649e-06
NOTCH1
[NCBI]
4.65204e-06
PAH
[NCBI]
4.18649e-06
HTT
[NCBI]
2.99023e-06
SOD1
[NCBI]
2.39949e-06
ACHE
[NCBI]
2.18853e-06
OMIM
OMIM
Link
Information
gain
01
homocystinuria
[NCBI]
0.00586721
methylmalonic aciduria and homocystinuria, cbld type
[NCBI]
0.00372806
methylmalonic aciduria and homocystinuria, cblc type
[NCBI]
0.00138371
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity
[NCBI]
0.00113232
homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type
[NCBI]
0.000873328
methylcobalamin deficiency, cblg type
[NCBI]
0.000396443
homocysteinemia
[NCBI]
0.000305856
MTHFR
[NCBI]
0.000287196
MFS
[NCBI]
0.000165465
MTRR
[NCBI]
0.000165289
MTR
[NCBI]
0.000141717
puerto rican infant hypotonia syndrome
[NCBI]
0.000101119
sulfocysteinuria
[NCBI]
7.70927e-05
mmachc gene
[NCBI]
7.25207e-05
neural tube defects, folate-sensitive
[NCBI]
6.11102e-05
transcobalamin ii deficiency
[NCBI]
3.1778e-05
contractural arachnodactyly, congenital
[NCBI]
2.70623e-05
ACHE
[NCBI]
8.15255e-08
Database Center for Life Science