Details of Disease

General Information of Disease (ID: DIS625V0)

• Disease Name: Inborn disorder of pyridoxine metabolism
• Synonyms: disorder of pyridoxine metabolism; inborn error of pyridoxine metabolic process; inborn pyridoxine metabolic process disorder; rare inborn error of pyridoxine metabolic process
• Definition: An inherited metabolic disease that is has its basis in the disruption of pyridoxine metabolic process.
• Disease Hierarchy:
  DISMXIZ8: Inborn disorder of biogenic amine metabolism and transport
  DISO5FAY: Inborn error of metabolism
  DISLXUF3: Inborn vitamin metabolic disorder
  DIS625V0: Inborn disorder of pyridoxine metabolism
• Disease Identifiers:
  MONDO ID: MONDO_0019237
  UMLS CUI: C5681285
  MedGen ID: 1842882
  Orphanet ID: 79192