Hartnup disorderOther Metabolites Mapped to 'Hartnup disease'HMDB0000929 (L-Tryptophan) HMDB0000197 (Indoleacetic acid)
- HMDB0000929 (L-Tryptophan)
- Hartnup disease
- 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.