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MeSH keywords -> Related genes, diseases (OMIM)


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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