Hartnup Disease

About the Disease
Hartnup Disorder, also known as hartnup disease, is related to aminoaciduria and cystinuria, and has symptoms including seizures An important gene associated with Hartnup Disorder is SLC6A19 (Solute Carrier Family 6 Member 19), and among its related pathways/superpathways are Disease and Transport of inorganic cations/anions and amino acids/oligopeptides. Affiliated tissues include Kidney, skin and cerebellum, and related phenotypes are hyperreflexia and eeg abnormality

Common Targets
SLC6A19

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