Hartnup disease

MONDO:0009324

Hartnup disease is a rare metabolic disorder belonging to the neutral aminoacidurias and characterized by abnormal renal and gastrointestinal transport of neutral amino acids (tryptophan, alanine, asparagine, glutamine, histidine, isoleucine, leucine, phenylalanine, serine, threonine, tyrosine and valine).

Also known as: Hartnup disease, Hartnup disorder, aminoaciduria, Hartnup type, HND

0 clinical trials for this condition and its sub-types, 0 tagged with Hartnup disease itself.

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↑ Inborn disorder of amino acid transport (16)

Including sub-types (0) Tagged with Hartnup disease (0)

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