Inborn disorder of aspartate family metabolism

MONDO:0037938

An inherited metabolic disease that is has its basis in the disruption of aspartate family amino acid metabolic process.

Also known as: inborn aspartate family amino acid metabolic process disorder, inborn error of aspartate family amino acid metabolic process, rare inborn error of aspartate family amino acid metabolic process

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

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Where it sits in the disease tree

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Part of

↑ Inborn errors of metabolism (2228)

Sub-types of Inborn disorder of aspartate family metabolism

Disorder of methionine catabolism 0 trials
3 sub-types
- Adenosine kinase deficiency 0 trials
- Glycine N-methyltransferase deficiency 0 trials
- Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase 0 trials
Inborn disorder of lysine and hydroxylysine metabolism 0 trials
5 sub-types
- 2-aminoadipic 2-oxoadipic aciduria 0 trials
- Hyperlysinemia 0 trials Sub-types →
- Inborn disorder of lysine, hydroxylysine, and tryptophan metabolism 0 trials
- Saccharopinuria 0 trials
- Seizures-intellectual disability due to hydroxylysinuria syndrome 0 trials

Most studied deeper sub-types

Hyperlysinemia due to defect in lysine transport into mitochondria (0)

Including sub-types (0) Tagged with Inborn disorder of aspartate family metabolism (0)

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