Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Dihydrolipoamide Dehydrogenase	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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