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CompoundsSubstances with curated findings
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ProteinsTransporters and enzymes
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Reference

Evidence

Compounds
Outcomes
Proteins
Interactions
Papers
Articles

Chemistry

Reactions
Reach

Reference layer

Pathways
Processes
Anatomy
Cell types
Organisms
Materials
Assessments
Diseases

Atlas Graph Twin Access

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Computational infrastructure for human biology, built on a provenance-aware knowledge graph. Findings retain their sources; research and simulation are the next layers.

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A reference for what the literature reports. Not medical advice.

Disease

inborn disorder of ornithine, proline and hydroxyproline metabolism

MONDO:0800156Mondo

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Findings

No curated finding names inborn disorder of ornithine, proline and hydroxyproline metabolism yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

A disorder of amino acid metabolism that has its basis in the disruption of the metabolism of ornithine, proline and/or hydroxyproline.

Definition from the Mondo Disease Ontology (MONDO:0800156), read 2026-09-29. CC BY 4.0.

Where it sits

A kind of: inborn disorder of amino acid metabolism