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type 1B Maple syrup urine disease

MSUD due to deficiency of e1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex

Also Known As:

Maple syrup urine disease, type 1B; MSUD1B; Maple Syrup Urine Disease, Type IB

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

Disease Context: Research Results

Nervous System Diseases: 14178
- Central Nervous System Diseases: 4213
  - Brain Diseases: 15694
    - Metabolic Brain Diseases: 215
      - Inborn Metabolic Brain Diseases: 2
        Maple Syrup Urine Disease: 712
        type 1B Maple syrup urine disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Inborn Metabolic Brain Diseases: 2
      - Maple Syrup Urine Disease: 712
        type 1B Maple syrup urine disease
    - Inborn Errors Amino Acid Metabolism: 1
      - Maple Syrup Urine Disease: 712
        type 1B Maple syrup urine disease
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Inborn Errors Metabolism: 1162
    - Inborn Metabolic Brain Diseases: 2
      - Maple Syrup Urine Disease: 712
        type 1B Maple syrup urine disease
    - Inborn Errors Amino Acid Metabolism: 1
      - Maple Syrup Urine Disease: 712
        type 1B Maple syrup urine disease
  - Metabolic Brain Diseases: 215
    - Inborn Metabolic Brain Diseases: 2
      - Maple Syrup Urine Disease: 712
        type 1B Maple syrup urine disease