Gilchrist type muscular dystrophy

disorder

SNOMED 240069003CUI C0410186

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Autosomal dominant muscular dystrophy with gene located at 5q31(parent)

Quick Facts

SNOMED CT: 240069003
UMLS CUI: C0410186
Fully Specified Name: Late onset proximal muscular dystrophy with dysarthria (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.