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Diseases / Metabolic disease/ Inborn errors of metabolism/ Inborn disorder of amino acid and other organic acid metabolism

Inborn disorder of lysine and hydroxylysine metabolism

rare

Identifiers: MONDO:0017351 Orphanet:289832
Part of: Inborn disorder of amino acid and other organic acid metabolism Inborn disorder of aspartate family metabolism

Subtypes

All diseases Rare only

Disease Rare Not rare Subtypes

Hyperlysinemia MONDO:0009388 AASS 1
2-aminoadipic 2-oxoadipic aciduria MONDO:0008774 DHTKD1
Inborn disorder of lysine, hydroxylysine, and tryptophan metabolism MONDO:0800157
Saccharopinuria MONDO:0010005
Seizures-intellectual disability due to hydroxylysinuria syndrome MONDO:0009373

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