- Compound
- CDB004871 (L-Tryptophan)
- Term
- Hartnup disease
- Definition
- An amino acid metabolic disorder that is caused by abnormalities of the renal tubules and is characterized especially by aminoaciduria involving only monocarboxylic monoamines, a dry red scaly rash, and episodic muscular incoordination due to the effects of the disease on the cerebellum. (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
Hartnup disorderOther Compounds Mapped to 'Hartnup disease'CDB004871 (L-Tryptophan)References