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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