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Reference

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A reference for what the literature reports. Not medical advice.

Disease

inborn disorder of serine family metabolism

MONDO:0019239Mondo

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Findings

No curated finding names inborn disorder of serine family metabolism yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

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

Definition from the Mondo Disease Ontology (MONDO:0019239), read 2026-09-29. CC BY 4.0.

Where it sits

A kind of: inborn disorder of amino acid and other organic acid metabolism
Narrower terms (3): glycine encephalopathy
inborn disorder of glycine and serine metabolism
neurometabolic disorder due to serine deficiency

Other names

4 names

Resolves to: inborn disorder of serine family metabolism

Also called: inborn disorder of serine or glycine metabolisminborn error of serine family amino acid metabolic processinborn serine family amino acid metabolic process disorderrare inborn error of serine family amino acid metabolic process