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Nemaline myopathy, early onset type

disorder
SNOMED 129621001CUI C1268589

Overview

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

Related Conditions

Typical nemaline myopathy(child)
Nemaline myopathy 3(child)
Intermediate nemaline myopathy(child)
Severe congenital nemaline myopathy(child)
Amish nemaline myopathy(child)
Nemaline myopathy(parent)
Congenital disease(parent)

Quick Facts

SNOMED CT
129621001
UMLS CUI
C1268589
Fully Specified Name
Nemaline myopathy, early onset type (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.