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CompoundsSubstances with curated findings
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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

PROM1-related retinopathy

MONDO:1040056Mondo

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Findings

No curated finding names PROM1-related retinopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Definition

Any retinopathy caused by variants in the PROM1 gene.

Definition from the Mondo Disease Ontology (MONDO:1040056), read 2026-09-29. CC BY 4.0.

Where it sits

A kind of: inherited retinal dystrophy
Narrower terms (3): cone-rod dystrophy 12
PROM1-related dominant retinopathy
PROM1-related recessive retinopathy