Hartnup disease
id:
hartnup-disease-162-8552762
title:
Hartnup disease
text:
Hartnup disease is an autosomal recessive metabolic disorder affecting the absorption of nonpolar amino acids. Niacin is a precursor to nicotinamide, a necessary component of NAD+. The causative gene, SLC6A19, is located on chromosome 5. It is named after the British family, Hartnup, who had this disease.
brand slug:
wiki
category slug:
encyclopedia
description:
Metabolic disorder
original url:
https://en.wikipedia.org/wiki/Hartnup_disease
date created:
2005-08-13T02:26:45Z
date modified:
2024-08-27T22:10:43Z
main entity:
{"identifier":"Q200985","url":"https://www.wikidata.org/entity/Q200985"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/b/b8/L-tryptophan-skeletal.png","width":1780,"height":1916}
fields total:
13
integrity:
16