Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:1060 - Hartnup disease

Disease Ontology 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.

Synonyms: Neutral 1 amino acid transport defect, Neutral 1 amino acid transport defect (disorder), deficiency of tryptophan oxygenase, neutral amino acid transport defect,

Xenbase Genes : slc6a19

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009324 - Hartnup disease


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): amino acid metabolic disorder (is_a)