Concept information
Preferred term
aminoacid disorder
Broader concept
Narrower concepts
- 3-hydroxy-3 methylglutaryl-CoA lyase deficiency
- albinism
- alcaptonuria
- biotidinase deficiency
- biotin-[propionyl-CoA-carboxylase (ATP-hydrolysing)] ligase deficiency
- carbamoyl phosphate synthetase deficiency
- carnosinemia
- citrullinemia
- cystathioninuria
- cystinosis
- cystinuria
- De Toni-Debre-Fanconi syndrome
- Hartnup disease
- histidinemia
- homocystinuria
- hyperalaninemia
- hyperaminoacidemia
- hyperaminoaciduria
- hyperargininemia
- hyperglycinemia
- hyperglycinuria
- hyperhomocysteinemia
- hyperlysinemia
- hypermethioninemia
- hyperornithinemia
- hyperphenylalaninemia
- hyperprebetalipoproteinemia
- hyperprolinemia
- hyperprolinuria
- hypersarcosinemia
- hypertyrosinemia
- iminoglycinuria
- Joseph disease
- leucinosis
- ornithine carbamoyltransferase deficiency
- phenylketonuria
- pyruvate carboxylase deficiency
- trimethylaminuria
- tyrosinemia
- xanthinuria
In other languages
-
French
URI
http://data.loterre.fr/ark:/67375/VH8-W790N3DT-N
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