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

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.