|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An amino acid metabolic disorder that iis 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. (Human Disease Ontology, DOID_1060)|
|Downloads & Tools|
1 genes/proteins associated with the disease Hartnup Disease from the curated CTD Gene-Disease Associations dataset.
|SLC6A19||solute carrier family 6 (neutral amino acid transporter), member 19||2.88009|