Home Page
References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 7/07/2006
Symbol HND
Location 5p15
Name Hartnup disorder
Corresponding gene SLC6A19
Main clinical features pellagro-like light-sensitive rash, cerebellar ataxia, emotional instability and amino-aciduria
Genetic determination autosomal recessive
Function/system disorder metabolism/aminoacids
Type disease
Gene product
Name solute carrier family 6 (neurotransmitter transporter), member 19