Congenital hypoplasia of fovea centralis

disorder

SNOMED 429449002CUI C1996981

Overview

Congenital hypoplasia of fovea centralis is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

O'Donnell Pappas syndrome(child)

Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome(child)

Congenital macular hypoplasia(parent)

Abnormality of fovea centralis morphology(parent)

Quick Facts

SNOMED CT: 429449002
UMLS CUI: C1996981
Fully Specified Name: Congenital hypoplasia of fovea centralis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.