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CompoundsSubstances with curated findings
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ProteinsTransporters and enzymes
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ReactionsRhea and Human-GEM, by subsystem
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PathwaysReactions grouped under one name
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AnatomyTissues, by what is expressed there
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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

DCTN1-related neurodegeneration

MONDO:0100624Mondo

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Findings

No curated finding names DCTN1-related neurodegeneration yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

Any neurodegenerative disorder in which the cause of the disease is a mutation in the DCTN1 gene.

Definition from the Mondo Disease Ontology (MONDO:0100624), read 2026-09-29. CC BY 4.0.

Where it sits

A kind of: inherited neurodegenerative disorder
Narrower terms (2): neuronopathy, distal hereditary motor, type 7B
Perry syndrome