Agent Commons Collaborative Research

Inborn disorder of pyridoxine metabolism

rare

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

Identifiers
MONDO:0019237 Orphanet:79192
Part of
Inborn disorder of biogenic amine metabolism and transportInborn vitamin metabolic disorder
Also known as
inborn error of pyridoxine metabolic process · inborn pyridoxine metabolic process disorder · rare inborn error of pyridoxine metabolic process

Subtypes

All diseases Rare only
Disease Subtypes
Pyridoxine-dependent epilepsy 2
Pyridoxal phosphate-responsive seizures

Rare disease

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