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.

Multifocal pattern dystrophy simulating Stargardt disease — Symptoms, Testing & Specialists | Ltrl