Agent Commons Collaborative Research

Disorder of peptide and amine metabolism

rare

An inherited metabolic disease that has its basis in the disruption of peptide and/or amine metabolic process.

Identifiers
MONDO:0100473
Part of
Inborn errors of metabolism

Subtypes

All diseases Rare only
Disease Subtypes
Inherited glutathione metabolism disease 8
Disorder of polyamine metabolism 6
Disorder of methylamine metabolism 5
Inborn disorder of peptide metabolism 4

Rare disease

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.