Hyperlysinemia

MONDO:0009388

Hyperlysinaemia is a lysine metabolism disorder characterized by elevated levels of lysine in the cerebrospinal fluid and blood. Variable degrees of saccharopinuria are also present.

Also known as: hyperlysinemia, hyperlysinemia (disease), hyperlysinemia type I, lysine alpha-ketoglutarate reductase deficiency, Alpha-aminoadipic semialdehyde synthase deficiency, L-lysine NAD-oxido-reductase deficiency, L-lysine:NAD-oxido-reductase deficiency, hyperlysinemia, type 1

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

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↑ Inborn disorder of amino acid metabolism (159) ↑ Inborn disorder of lysine and hydroxylysine metabolism (0)

Sub-types of Hyperlysinemia

Hyperlysinemia due to defect in lysine transport into mitochondria 0 trials

Including sub-types (0) Tagged with Hyperlysinemia (0)

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