Trait
Abnormal optical coherence tomography
Optical coherence tomography (OCT) is an optical method for cross-sectional imaging with a resolution approaching that of histopathology and a depth of penetration of a few mm. In ophthalmology, OCT has become a standard of care for retinal imaging. This term groups abnormal findings that are considered OCT-specific.
Summary
- Body system
- Abnormality of the eye
Reference genomeGRCh38hg38
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The Human Phenotype Ontology links no gene to Abnormal optical coherence tomography itself. The narrower traits below list theirs.
Narrower traits
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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