Hereditary retinal dystrophy primarily involving retinal pigment epithelium

disorder

SNOMED 698847000CUI C3698123

Overview

Hereditary retinal dystrophy primarily involving retinal pigment epithelium is a disorder.

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

Related Conditions

Biallelic RPE65 mutation associated retinal dystrophy(child)

Pattern dystrophy of macula(child)

Multifocal pattern dystrophy simulating Stargardt disease(child)

Reticular dystrophy of retinal pigment epithelium(child)

Hereditary retinal dystrophy(parent)

Retinal pigment epithelial dystrophy(parent)

Quick Facts

SNOMED CT: 698847000
UMLS CUI: C3698123
Fully Specified Name: Hereditary retinal dystrophy primarily involving retinal pigment epithelium (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.