Phénylcétonurie (Q194041)

De Wikidata
Aller à : navigation, rechercher
amino acid metabolic disorder that is characterized by a mutation in the gene for the hepatic enzyme phenylalanine hydroxylase (PAH), rendering it nonfunctionalanglais
  • Maladie de Følling
  • Phenylcetonurie
modifier
Langue Libellé Description Alias
français
Phénylcétonurie
Aucune description fournie
  • Maladie de Følling
  • Phenylcetonurie
anglais
phenylketonuria
amino acid metabolic disorder that is characterized by a mutation in the gene for the hepatic enzyme phenylalanine hydroxylase (PAH), rendering it nonfunctional
  • F?lling's disease
  • PKU
  • maternal phenylketonuria
  • phenylalaninemia
  • Følling's disease

Déclarations

Identifiants

 
modifier
    modifier
      modifier
        modifier
          modifier
            modifier
              modifier
                modifier