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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 |