MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Leigh Disease
[NCBI]
Gene
Gene
Link
Information
Gain
01
COX11P
[NCBI]
0.000415947
RNR2
[NCBI]
0.000283888
SURF1
[NCBI]
0.000219539
TRNL1
[NCBI]
0.000204011
ND5
[NCBI]
8.86944e-05
SCO2
[NCBI]
8.63185e-05
NDUFS7
[NCBI]
6.82105e-05
NDUFS4
[NCBI]
6.82105e-05
ATP6
[NCBI]
6.0802e-05
COX10
[NCBI]
4.76728e-05
NDUFS1
[NCBI]
4.0857e-05
LRPPRC
[NCBI]
3.75095e-05
NDUFS8
[NCBI]
3.69313e-05
NDUFV1
[NCBI]
3.64119e-05
SCO1
[NCBI]
3.59405e-05
ND3
[NCBI]
3.37702e-05
COX15
[NCBI]
2.72152e-05
NDUFA8
[NCBI]
2.6198e-05
SUCLA2
[NCBI]
2.33844e-05
SDHA
[NCBI]
2.21184e-05
PDHX
[NCBI]
1.9483e-05
SPG7
[NCBI]
1.91338e-05
COX4I1
[NCBI]
1.59767e-05
NDUFA2
[NCBI]
1.59767e-05
NDUFA11
[NCBI]
1.59767e-05
COX7A2L
[NCBI]
1.59767e-05
COX5A
[NCBI]
1.59767e-05
PET112L
[NCBI]
1.35963e-05
SURF4
[NCBI]
1.35963e-05
NDUFB6
[NCBI]
1.2698e-05
COX7A2
[NCBI]
1.2698e-05
COX11
[NCBI]
1.2698e-05
OXA1L
[NCBI]
1.21146e-05
COX17
[NCBI]
1.13353e-05
ATP5J
[NCBI]
1.10479e-05
NDUFA1
[NCBI]
1.10479e-05
NDUFS3
[NCBI]
1.10479e-05
NDUFS2
[NCBI]
1.05869e-05
BCS1L
[NCBI]
1.00678e-05
COX1
[NCBI]
9.79264e-06
COX2
[NCBI]
9.25219e-06
PCCB
[NCBI]
9.16192e-06
SFRS2
[NCBI]
8.84209e-06
PDHA1
[NCBI]
8.77067e-06
ND2
[NCBI]
8.77067e-06
FXN
[NCBI]
4.71608e-06
PTGS1
[NCBI]
2.9986e-06
OMIM
OMIM
Link
Information
gain
01
LS
[NCBI]
0.0073017
MTATP6
[NCBI]
0.00121211
cataract and cardiomyopathy
[NCBI]
0.00111789
SURF1
[NCBI]
0.00069135
mitochondrial complex iv deficiency
[NCBI]
0.000684255
mitochondrial complex i deficiency
[NCBI]
0.00043749
LSFC
[NCBI]
0.00035809
MTND5
[NCBI]
0.000337926
NDUFS8
[NCBI]
0.000230657
NDUFS4
[NCBI]
0.000197215
leigh syndrome, x-linked
[NCBI]
0.000178682
NDUFS1
[NCBI]
0.000153614
NDUFS7
[NCBI]
0.000153614
MTND6
[NCBI]
0.00014363
SNDI
[NCBI]
0.000133299
coenzyme q10 deficiency
[NCBI]
0.000126099
COX15
[NCBI]
0.000126062
apnea, central sleep
[NCBI]
0.000111707
KSS
[NCBI]
9.8708e-05
MTTK
[NCBI]
7.87471e-05
PDHA1
[NCBI]
7.81395e-05
PDSS2
[NCBI]
7.67296e-05
NDUFS3
[NCBI]
7.67296e-05
COX11
[NCBI]
7.67296e-05
COX7A2
[NCBI]
7.67296e-05
PET112L
[NCBI]
7.67296e-05
NDUFA8
[NCBI]
7.67296e-05
dystonia, familial, with visual failure and striatal lucencies
[NCBI]
6.79662e-05
mitochondrial complex ii deficiency
[NCBI]
6.52682e-05
SCO1
[NCBI]
6.29532e-05
NDUFB6
[NCBI]
6.29532e-05
pyruvate dehydrogenase e3-binding protein deficiency
[NCBI]
6.09456e-05
NDUFV1
[NCBI]
5.77562e-05
MTTV
[NCBI]
5.77562e-05
MTND3
[NCBI]
5.18754e-05
COX10
[NCBI]
5.18754e-05
MTTW
[NCBI]
5.18754e-05
SDHA
[NCBI]
4.98781e-05
humanin
[NCBI]
4.98781e-05
glutaric acidemia i
[NCBI]
4.84952e-05
leber optic atrophy
[NCBI]
4.73836e-05
SCO2
[NCBI]
4.67974e-05
PDHX
[NCBI]
4.67974e-05
BCS1L
[NCBI]
4.67974e-05
SDHC
[NCBI]
4.67974e-05
MTCO3
[NCBI]
4.67974e-05
DLD
[NCBI]
4.02693e-05
maple syrup urine disease
[NCBI]
2.90029e-05
panencephalitis, subacute sclerosing
[NCBI]
1.43016e-06
Database Center for Life Science