Hartnup disease

Summary
Synonym
  • Neutral 1 amino acid transport defect
  • deficiency of tryptophan oxygenase
  • 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.
Super Class
amino acid metabolic disorder
Disease Ontology
DOID:1060
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
340024 SLC6A19 solute carrier family 6 member 19
Displaying 1 entry
Gene ID Gene Symbol Description Source
74338 Slc6a19 solute carrier family 6 (neurotransmitter transporter), member 19
Displaying 1 entry
Gene ID Gene Symbol Description Source
664630 Slc6a19 solute carrier family 6 member 19

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024