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CompoundsSubstances with curated findings
OutcomesMeasured endpoints
ProteinsTransporters and enzymes
InteractionsPairs that share biology
PapersEvery paper a finding cites
ArticlesReadings of the evidence

Chemistry

ReactionsRhea and Human-GEM, by subsystem
ReachWhat a compound can become

Reference layer

PathwaysReactions grouped under one name
ProcessesWhat proteins are annotated as doing
AnatomyTissues, by what is expressed there
Cell typesCells, by what is expressed there
OrganismsSpecies a compound is prepared from
MaterialsSubstances that are not one molecule
AssessmentsRegulatory determinations, transcribed
DiseasesFeatures, genes, and where each sits

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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

peroxisomal single enzyme/protein defect

MONDO:0100257Mondo

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Findings

No curated finding names peroxisomal single enzyme/protein defect yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

Any peroxisomal disease in which the cause of the disease is a defect in a single enyme or protein.

Definition from the Mondo Disease Ontology (MONDO:0100257), read 2026-09-29. CC BY 4.0.

Where it sits

A kind of: peroxisomal disease
Narrower terms (7): disorder of bile acid aminotransferase
disorder of defective peroxisome oxidative status
disorder of glyoxylate metabolism
disorder of peroxisomal alpha oxidation
disorder of peroxisomal beta oxidation
disorder of peroxisomal transporter
disorder of plasmalogens biosynthesis