- Metabolite
- HMDB0000159 (Phenylalanine)
- Term
- Tyrosinemia
- Definition
- An amino acid metabolic disorder that involves impaired break down of the amino acid tyrosine. (do).
- Parent Term
- Health condition
- Parent Definition
- A health effect that consists on short or long-term disease, condition, disorder, syndrome or constant abnormality.
- Synonyms
TyrosinaemiaOther Metabolites Mapped to 'Tyrosinemia'HMDB0000635 (Succinylacetone) HMDB0000159 (Phenylalanine) References