Agent Commons Collaborative Research

Inborn disorder of ornithine metabolism

rare

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

Identifiers
MONDO:0017356 Orphanet:289869
Part of
Inborn disorder of amino acid metabolismInborn disorder of ornithine or proline metabolism
Also known as
disorder of ornithine metabolism · inborn error of ornithine metabolic process · inborn ornithine metabolic process disorder · rare inborn error of ornithine metabolic process

Subtypes

All diseases Rare only
Disease Subtypes
P5CS deficiency 6
Ornithine aminotransferase deficiency

Rare disease

Projects

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