Disease & disorder

inborn disorder of pyridoxine metabolism

MONDO:0019237

An inherited metabolic disease that is has its basis in the disruption of pyridoxine metabolic process.

Outbreak surveillance

Global reported events

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Clinical trials0
Recruiting0
Drug concepts studied0
Synonyms3
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Background context

inborn disorder of pyridoxine metabolism

Wikidata Q55788558 ↗
Background only. Canonical identity remains MONDO; clinical-trial relationships come from ClinicalTrials.gov.

Drugs being studied

Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.