Human genes for Hartnup disease
Hartnup disease [DOID:1060]
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.
Synonyms: Hartnup disease, DOID:1060, Hartnup disorder, Hartnup syndrome, Hartnup diseases ...
Linkouts: OMIM