Details of Disease

General Information of Disease (ID: DISNLMCZ)

• Disease Name: Inborn disorder of phenylalanine and tyrosine metabolism
• Synonyms: disorder of phenylalanin or tyrosine metabolism; inborn disorder of phenylalanin or tyrosine metabolism
• Disease Hierarchy:
  DISFWXCM: Inborn disorder of amino acid metabolism
  DISNLMCZ: Inborn disorder of phenylalanine and tyrosine metabolism
• Disease Identifiers:
  MONDO ID: MONDO_0019235
  UMLS CUI: C5681284
  MedGen ID: 1842953
  Orphanet ID: 79190