inborn disorder of pyridoxine metabolism
MONDO:0019237Mondo
Findings
No curated finding names inborn disorder of pyridoxine 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 pyridoxine metabolic process.
Definition from the Mondo Disease Ontology (MONDO:0019237), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
3 names
Resolves to: inborn disorder of pyridoxine metabolism
- Also called
- inborn error of pyridoxine metabolic processinborn pyridoxine metabolic process disorderrare inborn error of pyridoxine metabolic process