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Due To Atp Synthase Deficiency Neonatal Mitochondrial Encephalocardiomyopathy

mutations in TMEM70

Also Known As:

Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency

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

Disease Context: Research Results

Musculoskeletal Diseases: 719
- Muscular Diseases: 10128
  - Mitochondrial Myopathies: 872
    - Mitochondrial Encephalomyopathies: 427
      - Due To Atp Synthase Deficiency Neonatal Mitochondrial Encephalocardiomyopathy
Nervous System Diseases: 14178
- Central Nervous System Diseases: 4213
  - Brain Diseases: 15694
    - Metabolic Brain Diseases: 215
      - Mitochondrial Encephalomyopathies: 427
        Due To Atp Synthase Deficiency Neonatal Mitochondrial Encephalocardiomyopathy
- Neuromuscular Diseases: 2005
  - Muscular Diseases: 10128
    - Mitochondrial Myopathies: 872
      - Mitochondrial Encephalomyopathies: 427
        Due To Atp Synthase Deficiency Neonatal Mitochondrial Encephalocardiomyopathy
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Mitochondrial Diseases: 21919
    - Mitochondrial Myopathies: 872
      - Mitochondrial Encephalomyopathies: 427
        Due To Atp Synthase Deficiency Neonatal Mitochondrial Encephalocardiomyopathy
  - Metabolic Brain Diseases: 215
    - Mitochondrial Encephalomyopathies: 427
      - Due To Atp Synthase Deficiency Neonatal Mitochondrial Encephalocardiomyopathy
Enzymes and Coenzymes: 1
- Enzymes: 152586
Amino Acids, Peptides, and Proteins: 1
- Proteins: 484843