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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



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