phenylketonuria (Q194041)

From Wikidata
Jump to navigation Jump to search
amino acid metabolic disorder that is characterized by a mutation in the gene for the hepatic enzyme phenylalanine hydroxylase (PAH), rendering it nonfunctional
  • PKU
  • phenylalaninemia
  • Følling's disease
  • phenylketonurias
edit
Language Label Description Also known as
English
phenylketonuria
amino acid metabolic disorder that is characterized by a mutation in the gene for the hepatic enzyme phenylalanine hydroxylase (PAH), rendering it nonfunctional
  • PKU
  • phenylalaninemia
  • Følling's disease
  • phenylketonurias

Statements

Phenylketonuria testing.jpg
2,823 × 1,563; 972 KB
blood from a two‐week‐old being collected for phenylketonuria screening (English)
0 references
PKU (English)
0 references
PKU (German)
0 references
ΦΚΟ (Greek)
0 references
Phenylketonuria
0 references

Identifiers

fenylketonurie
0 references
0 references
0 references
0 references
0 references
5C50.0
Phenylketonuria
0 references
0 references
0 references
0 references
0 references
0 references
Phenylketonuria
0 references
0 references
0 references
14530977-n
1 reference
 
edit
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit