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Deafness, nonsyndromic sensorineural, mitochondrial
Deafness, nonsyndromic sensorineural, mitochondrial
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
DEAFNESS, NONSYNDROMIC SENSORINEURAL, MITOCHONDRIAL
C3151897
COX1
Unknown
—
Disgenet
Oxidative phosphorylation
Metabolic pathways
Cardiac muscle contraction
Thermogenesis
Non-alcoholic fatty liver disease
Alzheimer disease
Parkinson disease
Amyotrophic lateral sclerosis
Huntington disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Chemical carcinogenesis - reactive oxygen species
Diabetic cardiomyopathy
TP53 Regulates Metabolic Genes
Respiratory electron transport
+12 more
ND1
Unknown
—
Disgenet
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
POU3F4
Unknown
—
Disgenet
—
All
3
Causal
0
Unknown
3
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
3
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
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Deafness, sensorineural, autosomal-mitochondrial type
2 shared genes
ND1, COX1
Related via 2 shared genes including ND1, COX1.
Deafness, aminoglycoside-induced
2 shared genes
ND1, COX1
Related via 2 shared genes including ND1, COX1.
Ayazi syndrome
1 shared gene
POU3F4
Related via 1 shared gene including POU3F4.
Choroideremia-deafness-obesity syndrome
1 shared gene
POU3F4
Related via 1 shared gene including POU3F4.
Chromosome xq21 deletion syndrome
1 shared gene
POU3F4
Related via 1 shared gene including POU3F4.
1
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