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Inborn disorder of lysine and hydroxylysine metabolism

MONDO:0017351

Also known as: disorder of lysine and hydroxylysine metabolism

0 clinical trials for this condition and its sub-types, 0 tagged with Inborn disorder of lysine and hydroxylysine metabolism itself.

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Part of

↑ Inborn disorder of amino acid and other organic acid metabolism (225) ↑ Inborn disorder of aspartate family metabolism (0)

Sub-types of Inborn disorder of lysine and hydroxylysine metabolism

2-aminoadipic 2-oxoadipic aciduria 0 trials
Hyperlysinemia 0 trials
1 sub-type
- Hyperlysinemia due to defect in lysine transport into mitochondria 0 trials
Inborn disorder of lysine, hydroxylysine, and tryptophan metabolism 0 trials
Saccharopinuria 0 trials
Seizures-intellectual disability due to hydroxylysinuria syndrome 0 trials

Including sub-types (0) Tagged with Inborn disorder of lysine and hydroxylysine metabolism (0)

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