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Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome
Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome
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Subtype of:
Mitochondrial encephalomyopathy
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome
MONDO_0010789
ND1
Unknown
11781695
8723687
1323207
17400793
12509858
9299505
15767514
Open Targets
Oxidative phosphorylation
Metabolic pathways
Thermogenesis
Retrograde endocannabinoid signaling
Alzheimer disease
Parkinson disease
Amyotrophic lateral sclerosis
Huntington disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Chemical carcinogenesis - reactive oxygen species
Diabetic cardiomyopathy
Respiratory electron transport
Complex I biogenesis
+11 more
ND4
Unknown
12509858
15767514
9299505
17400793
1323207
11781695
8723687
Open Targets
Oxidative phosphorylation
Metabolic pathways
Thermogenesis
Retrograde endocannabinoid signaling
Alzheimer disease
Parkinson disease
Amyotrophic lateral sclerosis
Huntington disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Chemical carcinogenesis - reactive oxygen species
Diabetic cardiomyopathy
Respiratory electron transport
Complex I biogenesis
+11 more
ND5
Unknown
12509858
1323207
8723687
17400793
9299505
15767514
11781695
Open Targets
Oxidative phosphorylation
Metabolic pathways
Thermogenesis
Retrograde endocannabinoid signaling
Alzheimer disease
Parkinson disease
Amyotrophic lateral sclerosis
Huntington disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Chemical carcinogenesis - reactive oxygen species
Diabetic cardiomyopathy
Respiratory electron transport
Complex I biogenesis
+11 more
ND6
Unknown
17400793
11781695
8723687
12509858
15767514
9299505
1323207
Open Targets
Oxidative phosphorylation
Metabolic pathways
Thermogenesis
Retrograde endocannabinoid signaling
Alzheimer disease
Parkinson disease
Amyotrophic lateral sclerosis
Huntington disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Chemical carcinogenesis - reactive oxygen species
Diabetic cardiomyopathy
Respiratory electron transport
Complex I biogenesis
+11 more
All
4
Causal
0
Unknown
4
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Open Targets
4
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5
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Congenital cardiomyopathy
2 shared genes
ND5, ND4
Related via 2 shared genes including ND5, ND4.
Melas syndrome
4 shared genes
ND1, ND6, ND5, ND4
Related via 4 shared genes including ND1, ND6, ND5.
Neuropathy, ataxia, and retinitis pigmentosa
3 shared genes
ND1, ND5, ND4
Related via 3 shared genes including ND1, ND5, ND4.
External ophthalmoplegia
1 shared gene
ND1
Related via 1 shared gene including ND1.
Cleft palate and bilateral cleft lip
3 shared genes
ND1, ND5, ND4
Related via 3 shared genes including ND1, ND5, ND4.
1
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