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MeSH keywords -> Related genes, diseases (OMIM)


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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