OBO ID: DOID:1060
Term Name: Hartnup disease Search Ontology:
Synonyms:
  • deficiency of tryptophan oxygenase
  • Neutral 1 amino acid transport defect
  • neutral amino acid transport defect
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. http://www2.merriam-webster.com/cgi-bin/mwmednlm?book=Medical&va=Hartnup
References:
Ontology: Human Disease   (DOID:1060)
OTHER Hartnup disease PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SLC6A19 Hartnup disorder 234500
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None