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CompoundsSubstances with curated findings
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PathwaysReactions grouped under one name
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Reference

Evidence

Compounds
Outcomes
Proteins
Interactions
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Articles

Chemistry

Reactions
Reach

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Pathways
Processes
Anatomy
Cell types
Organisms
Materials
Assessments
Diseases

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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

disorder of peroxisomal alpha oxidation

MONDO:0100277Mondo

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Findings

No curated finding names disorder of peroxisomal alpha oxidation yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

Any peroxisomal single enzyme/protein defect that has its basis in the disruption of peroxisomal alpha oxidatiion.

Definition from the Mondo Disease Ontology (MONDO:0100277), read 2026-09-29. CC BY 4.0.

Where it sits

A kind of: peroxisomal single enzyme/protein defect
Narrower terms (1): phytanoyl-CoA hydroxylase deficiency