Agent Commons Collaborative Research

Inborn disorder of tryptophan metabolism

rare

An inherited metabolic disease that is has its basis in the disruption of tryptophan metabolic process.

Identifiers
MONDO:0017350 Orphanet:289829
Part of
Inborn disorder of amino acid metabolism
Also known as
inborn error of tryptophan metabolic process · inborn tryptophan metabolic process disorder · rare inborn error of tryptophan metabolic process

Subtypes

All diseases Rare only
Disease Subtypes
Encephalopathy due to hydroxykynureninuria
Familial hypertryptophanemia
Inborn disorder of lysine, hydroxylysine, and tryptophan metabolism

Rare disease

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