MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Cytochrome-c Oxidase Deficiency
[NCBI]
Gene
Gene
Link
Information
Gain
01
COX7AP1
[NCBI]
0.000438875
COX7AP2
[NCBI]
0.000438875
TRNL1
[NCBI]
0.000226878
SCO2
[NCBI]
0.00020466
SURF1
[NCBI]
0.000115874
SCO1
[NCBI]
0.000101432
COX10
[NCBI]
6.5023e-05
COX15
[NCBI]
2.84531e-05
LRPPRC
[NCBI]
2.4622e-05
COX1
[NCBI]
2.33558e-05
TFAM
[NCBI]
1.89425e-05
COX19
[NCBI]
1.65908e-05
FASTKD2
[NCBI]
1.65908e-05
COX7A2L
[NCBI]
1.65908e-05
COX6A2
[NCBI]
1.42104e-05
COX16
[NCBI]
1.42104e-05
COX6A1
[NCBI]
1.42104e-05
SURF4
[NCBI]
1.42104e-05
COX6B1
[NCBI]
1.42104e-05
COX7A1
[NCBI]
1.3312e-05
COX7A2
[NCBI]
1.3312e-05
FXN
[NCBI]
1.30254e-05
PUS1
[NCBI]
1.22948e-05
COX17
[NCBI]
1.19492e-05
CYTB
[NCBI]
1.00617e-05
COX2
[NCBI]
9.86543e-06
SPG7
[NCBI]
8.95279e-06
TYMP
[NCBI]
7.72566e-06
OPA1
[NCBI]
7.0373e-06
ATP7A
[NCBI]
6.18124e-06
CYP2D6
[NCBI]
5.87962e-06
SMN1
[NCBI]
5.27998e-06
UCP3
[NCBI]
5.03218e-06
HMOX1
[NCBI]
4.41874e-06
SOD1
[NCBI]
2.94067e-06
GFAP
[NCBI]
1.9015e-06
CASP3
[NCBI]
1.39804e-06
OMIM
OMIM
Link
Information
gain
01
mitochondrial complex iv deficiency
[NCBI]
0.00275817
LS
[NCBI]
0.00231876
LSFC
[NCBI]
0.000626614
SURF1
[NCBI]
0.000582628
KSS
[NCBI]
0.000290896
SCO2
[NCBI]
0.000280964
MTCO1
[NCBI]
0.000238904
mitochondrial dna depletion syndrome, hepatocerebral form
[NCBI]
0.000223663
LIMM
[NCBI]
0.000201267
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency
[NCBI]
0.000177697
COX15
[NCBI]
0.00013984
MTTW
[NCBI]
0.000133953
MTCO3
[NCBI]
0.00012269
MTCO2
[NCBI]
0.000110347
COX7A3
[NCBI]
8.35435e-05
LRPPRC
[NCBI]
8.35435e-05
MLASA
[NCBI]
7.54786e-05
SCO1
[NCBI]
6.9765e-05
COX7A1
[NCBI]
6.9765e-05
mitochondrial myopathy with diabetes
[NCBI]
6.72141e-05
wolfram syndrome, mitochondrial form
[NCBI]
6.72141e-05
ETHE1
[NCBI]
6.45657e-05
MTTV
[NCBI]
6.45657e-05
PGAM1
[NCBI]
6.11901e-05
PUS1
[NCBI]
6.11901e-05
MERRF
[NCBI]
5.89884e-05
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive
[NCBI]
5.89884e-05
PCK2
[NCBI]
5.86805e-05
COX10
[NCBI]
5.86805e-05
mitochondrial dna depletion syndrome, myopathic form
[NCBI]
5.77528e-05
phosphoglycerate mutase, muscle, deficiency of
[NCBI]
5.50187e-05
MNGIE
[NCBI]
5.03074e-05
cutis laxa, x-linked
[NCBI]
4.82273e-05
mitochondrial complex i deficiency
[NCBI]
4.63923e-05
CYP2D6
[NCBI]
4.63915e-05
MTTS1
[NCBI]
4.51891e-05
WFS1
[NCBI]
3.84557e-05
MTTL1
[NCBI]
3.01559e-05
menkes disease
[NCBI]
2.85571e-05
SOD2
[NCBI]
1.54706e-05
GFAP
[NCBI]
2.02163e-06
Database Center for Life Science