MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Dihydrolipoamide Dehydrogenase
[NCBI]
Gene
Gene
Link
Information
Gain
01
DLD
[NCBI]
7.31456e-05
PDHX
[NCBI]
8.29422e-06
ACHE
[NCBI]
8.2855e-06
CS
[NCBI]
7.82705e-06
MPO
[NCBI]
6.32122e-06
VIP
[NCBI]
4.86935e-06
DLST
[NCBI]
4.1521e-06
DBT
[NCBI]
3.98608e-06
ARSA
[NCBI]
3.35828e-06
ESD
[NCBI]
2.78037e-06
VKORC1
[NCBI]
2.74602e-06
CYBB
[NCBI]
2.52441e-06
RELN
[NCBI]
2.43827e-06
DIAPH3
[NCBI]
2.08677e-06
OGDH
[NCBI]
2.08677e-06
PDHB
[NCBI]
1.84934e-06
SEPW1
[NCBI]
1.84934e-06
DLAT
[NCBI]
1.80144e-06
PGP
[NCBI]
1.78446e-06
CYB5R3
[NCBI]
1.68866e-06
CHAT
[NCBI]
1.68823e-06
PDHA1
[NCBI]
1.6666e-06
ASL
[NCBI]
1.55557e-06
TH
[NCBI]
1.37395e-06
NQO1
[NCBI]
1.10604e-06
DBH
[NCBI]
1.07219e-06
GDNF
[NCBI]
1.03718e-06
MB
[NCBI]
1.02362e-06
NOS1
[NCBI]
1.01254e-06
HTT
[NCBI]
9.04348e-07
EGF
[NCBI]
8.51825e-07
NOS3
[NCBI]
6.57154e-07
NPY
[NCBI]
4.52746e-07
OMIM
OMIM
Link
Information
gain
01
DLD
[NCBI]
0.00109656
maple syrup urine disease
[NCBI]
0.00103971
methemoglobinemia due to deficiency of methemoglobin reductase
[NCBI]
0.000548182
DIA3
[NCBI]
0.000202495
FRDA
[NCBI]
0.000169356
carnitine acetyltransferase deficiency
[NCBI]
0.000161049
PMC
[NCBI]
0.000108978
blood group, p system
[NCBI]
0.000103444
NQO1
[NCBI]
8.98095e-05
DIA2
[NCBI]
8.65913e-05
LS
[NCBI]
6.91354e-05
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency
[NCBI]
6.78488e-05
ACHE
[NCBI]
4.11757e-05
ARSA
[NCBI]
3.74724e-05
MPO
[NCBI]
3.33797e-05
CJD
[NCBI]
2.35079e-05
DBT
[NCBI]
2.17678e-05
VIP
[NCBI]
2.05989e-05
PGP
[NCBI]
2.00164e-05
NOS2A
[NCBI]
1.94854e-05
RELN
[NCBI]
1.73122e-05
ASL
[NCBI]
1.51617e-05
H6PD
[NCBI]
1.39312e-05
ASS
[NCBI]
1.28484e-05
HD
[NCBI]
5.75096e-06
GAL
[NCBI]
5.61642e-06
MB
[NCBI]
5.11271e-06
CHAT
[NCBI]
4.44988e-06
ADCYAP1
[NCBI]
3.70502e-06
HBB
[NCBI]
2.47393e-06
EGF
[NCBI]
2.11648e-06
TH
[NCBI]
1.01003e-06
NPY
[NCBI]
6.33093e-07
Database Center for Life Science