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MeSH keywords -> Related genes, diseases (OMIM)


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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