Multifocal pattern dystrophy simulating Stargardt disease

disorder

SNOMED 723408004CUI C4509881

Overview

Multifocal pattern dystrophy simulating Stargardt disease is a disorder.

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

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary retinal dystrophy primarily involving retinal pigment epithelium(parent)

Quick Facts

SNOMED CT: 723408004
UMLS CUI: C4509881
Fully Specified Name: Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus (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.