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

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