inborn disorder of aspartate family metabolism
MONDO:0037938Mondo
Findings
No curated finding names inborn disorder of aspartate 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 aspartate family amino acid metabolic process.
Definition from the Mondo Disease Ontology (MONDO:0037938), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
3 names
Resolves to: inborn disorder of aspartate family metabolism
- Also called
- inborn aspartate family amino acid metabolic process disorderinborn error of aspartate family amino acid metabolic processrare inborn error of aspartate family amino acid metabolic process