MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Acidosis, Lactic
[NCBI]
Gene
Gene
Link
Information
Gain
01
PDHX
[NCBI]
4.85607e-05
PDHA1
[NCBI]
3.55862e-05
NDUFV1
[NCBI]
2.4897e-05
BCS1L
[NCBI]
2.4897e-05
DLD
[NCBI]
2.45975e-05
POLG
[NCBI]
1.71845e-05
UQCRB
[NCBI]
1.70688e-05
SUCLG1
[NCBI]
1.46884e-05
SLC25A3
[NCBI]
1.37899e-05
ISCU
[NCBI]
1.32065e-05
PPM2C
[NCBI]
1.32065e-05
LDHD
[NCBI]
1.27727e-05
TPK1
[NCBI]
1.27727e-05
PUS1
[NCBI]
1.27727e-05
NDUFA8
[NCBI]
1.27727e-05
NDUFS1
[NCBI]
1.24271e-05
ABCB6
[NCBI]
1.21396e-05
NDUFS2
[NCBI]
1.16784e-05
PDHB
[NCBI]
1.16784e-05
NDUFS7
[NCBI]
1.14873e-05
SLC19A3
[NCBI]
1.14873e-05
DNM1L
[NCBI]
1.1016e-05
CYTB
[NCBI]
1.05393e-05
ND5
[NCBI]
1.00851e-05
SFRS2
[NCBI]
9.93253e-06
SLC25A4
[NCBI]
9.6629e-06
ND1
[NCBI]
8.99917e-06
SLC25A13
[NCBI]
8.83776e-06
PC
[NCBI]
8.49047e-06
ACCN4
[NCBI]
7.7602e-06
SLC19A2
[NCBI]
7.68018e-06
CS
[NCBI]
7.13336e-06
ACP5
[NCBI]
4.39532e-06
LIF
[NCBI]
4.236e-06
IL10
[NCBI]
3.66858e-06
ACHE
[NCBI]
3.16621e-06
TNF
[NCBI]
2.79133e-06
PTGS2
[NCBI]
1.44179e-06
OMIM
OMIM
Link
Information
gain
01
cataract and cardiomyopathy
[NCBI]
0.00502949
MELAS
[NCBI]
0.00114443
succinic acidemia
[NCBI]
0.00111789
MEHMO
[NCBI]
0.000764597
myopathy with deficiency of succinate dehydrogenase and aconitase
[NCBI]
0.000667246
pyruvate decarboxylase deficiency
[NCBI]
0.0006205
gracile syndrome
[NCBI]
0.000594161
MTTL1
[NCBI]
0.000496105
pyruvate dehydrogenase e3-binding protein deficiency
[NCBI]
0.000376644
LS
[NCBI]
0.000357174
PDHX
[NCBI]
0.000261156
PDHA1
[NCBI]
0.000254792
mitochondrial complex i deficiency
[NCBI]
0.000202888
pyruvate dehydrogenase phosphatase deficiency
[NCBI]
0.000183322
MLASA
[NCBI]
0.000183322
LSFC
[NCBI]
0.000164976
alpha-ketoglutarate dehydrogenase deficiency
[NCBI]
0.000138764
pearson marrow-pancreas syndrome
[NCBI]
0.000138178
PUS1
[NCBI]
0.000130189
MTND4
[NCBI]
0.000121345
mitochondrial phosphate carrier deficiency
[NCBI]
0.000118781
BCS1L
[NCBI]
0.000113044
MTCO3
[NCBI]
0.000113044
mitochondrial complex iv deficiency
[NCBI]
0.000112981
MTCO2
[NCBI]
0.000100709
adrenoleukodystrophy, autosomal neonatal form
[NCBI]
0.00010032
DLD
[NCBI]
9.92366e-05
pyruvate dehydrogenase e2 deficiency
[NCBI]
9.63185e-05
atpaf2 deficiency
[NCBI]
9.63185e-05
SLC25A4
[NCBI]
9.11904e-05
MTATP6
[NCBI]
7.89406e-05
DNM1L
[NCBI]
7.8776e-05
SUCLG1
[NCBI]
7.8776e-05
UQCRB
[NCBI]
7.8776e-05
mitochondrial complex iii deficiency
[NCBI]
7.50102e-05
encephalopathy, ethylmalonic
[NCBI]
7.50102e-05
lactic acidosis, fatal infantile
[NCBI]
6.99932e-05
KSS
[NCBI]
6.65815e-05
SLC25A3
[NCBI]
6.49988e-05
MERRF
[NCBI]
6.17575e-05
NDUFV1
[NCBI]
5.98009e-05
BNIP3
[NCBI]
5.98009e-05
mitochondrial dna depletion syndrome, hepatocerebral form
[NCBI]
5.83006e-05
pyruvate carboxylase deficiency
[NCBI]
5.23319e-05
SURF1
[NCBI]
4.30113e-05
3-@hydroxy-3-methylglutaryl-coa lyase deficiency
[NCBI]
3.88823e-05
ACADS
[NCBI]
3.75351e-05
MTND1
[NCBI]
3.59867e-05
MTTK
[NCBI]
3.43437e-05
PC
[NCBI]
2.96474e-05
glycogen storage disease i
[NCBI]
2.8593e-05
OPMD
[NCBI]
2.46403e-05
PTHLH
[NCBI]
8.76718e-06
VEGF
[NCBI]
7.99156e-06
TNF
[NCBI]
6.00577e-06
RP
[NCBI]
4.04492e-06
ACHE
[NCBI]
2.26466e-06
Database Center for Life Science