Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Succinate Cytochrome c Oxidoreductase [NCBI]

Gene


 Gene Link Information
Gain		 01
CS [NCBI] 3.77714e-06
UQCRQ [NCBI] 2.77693e-06
COQ2 [NCBI] 2.6241e-06
CYC1 [NCBI] 2.44447e-06
ASS1 [NCBI] 2.32245e-06
OXA1L [NCBI] 2.15452e-06
CYCS [NCBI] 2.13889e-06
HTT [NCBI] 1.46309e-06
GAPDH [NCBI] 1.43963e-06
SNCA [NCBI] 1.40388e-06



OMIM


 OMIM Link Information
gain		 01
mitochondrial complex ii deficiency [NCBI] 0.000303596
wolfram syndrome, mitochondrial form [NCBI] 0.000303596
WFS1 [NCBI] 0.000230117
diarrhea, chronic, with villous atrophy [NCBI] 0.000198366
NN [NCBI] 0.000166778
mitochondrial myopathy [NCBI] 0.000132967
mitochondrial dna depletion syndrome, hepatocerebral form [NCBI] 0.000110418
MELAS [NCBI] 0.000104707
mitochondrial complex iv deficiency [NCBI] 9.43614e-05
SDHC [NCBI] 8.09294e-05
KSS [NCBI] 6.75721e-05
MPV17 [NCBI] 4.21038e-05
MTTF [NCBI] 4.01292e-05
PCK2 [NCBI] 4.01292e-05
MTTI [NCBI] 3.80948e-05
MTTK [NCBI] 3.11904e-05
MTCYB [NCBI] 2.98289e-05
GAPDH [NCBI] 1.38373e-05



Database Center for Life Science