Details of Disease

General Information of Disease (ID: DIS0WTSJ)

• Disease Name: Inborn disorder of aspartate family metabolism
• Synonyms: rare inborn error of aspartate family amino acid metabolic process; inborn aspartate family amino acid metabolic process disorder; inborn error of aspartate family amino acid metabolic process
• Definition: An inherited metabolic disease that is has its basis in the disruption of aspartate family amino acid metabolic process.
• Disease Hierarchy:
  DISFWXCM: Inborn disorder of amino acid metabolism
  DISO5FAY: Inborn error of metabolism
  DISTVTFI: Disorder of organic acid metabolism
  DISWE0E0: Inborn disorder of amino acid and other organic acid metabolism
  DIS0WTSJ: Inborn disorder of aspartate family metabolism