5 Autosomal Dominant Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions

aka PEOA5; mutations in RRM2B

Also Known As:

Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5; Peoa5; Progressive External Ophthalmoplegia, Autosomal Dominant, 5

Networked: 0 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Musculoskeletal Diseases: 719
- Muscular Diseases: 10128
  - Mitochondrial Myopathies: 872
    - Chronic Progressive External Ophthalmoplegia: 575
      - 5 Autosomal Dominant Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions
Nervous System Diseases: 14178
Eye Diseases: 3522
- Ocular Motility Disorders: 514
  - Ophthalmoplegia: 867
    - Chronic Progressive External Ophthalmoplegia: 575
      - 5 Autosomal Dominant Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Mitochondrial Diseases: 21919
    - Mitochondrial Myopathies: 872
      - Chronic Progressive External Ophthalmoplegia: 575
        5 Autosomal Dominant Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions
    - 5 Autosomal Dominant Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions
Signs and Symptoms Pathological Conditions
- Pathologic Processes: 10023
  - Disease Attributes: 18
    - Chronic Disease: 25762
      - Chronic Progressive External Ophthalmoplegia: 575
        5 Autosomal Dominant Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions
- Signs and Symptoms
  - Neurologic Manifestations: 7102
    - Paralysis: 14164
      - Ophthalmoplegia: 867
        Chronic Progressive External Ophthalmoplegia: 575
        5 Autosomal Dominant Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions