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Retinal dystrophy due to GM2 gangliosidosis

disorder
SNOMED 1187543005CUI C5569064

Overview

Retinal dystrophy due to GM2 gangliosidosis is a disorder.

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

Related Conditions

Retinal dystrophy(parent)

Quick Facts

SNOMED CT
1187543005
UMLS CUI
C5569064
Fully Specified Name
Dystrophy of retina due to GM2 gangliosidosis (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.