Hartnup Disease Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006250
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1 genes/proteins associated with the disease Hartnup Disease from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SLC6A19 solute carrier family 6 (neutral amino acid transporter), member 19 2.88009