Diseases Associated With Mitochondrial Genome Maintenance
| Disease |
|
Mitochondrial Diseases
|
|
Cochlear Diseases
|
|
Coronary Artery Disease, Autosomal Dominant, 1
|
|
Diabetic Cardiomyopathies
|
|
Emaciation
|
|
Focal Segmental Glomerulosclerosis
|
|
Liver Cirrhosis, Experimental
|
|
Malformations Of Cortical Development
|
|
Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome
|
|
Ophthalmoplegia
|
|
Optic Atrophy 1 And Deafness
|
|
Optic Atrophy, Autosomal Dominant
|
|
Osteoarthritis
|
|
Pigmentation Disorders
|
|
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 1
|
|
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 2
|
|
Proteinuria
|
|
Cardiomyopathy, Familial Hypertrophic, 1
|
|
Respiratory Insufficiency
|
