Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome

disorder

SNOMED 724349009CUI C4510610

Overview

Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome is a disorder.

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

Related Conditions

Autosomal dominant hereditary disorder(parent)

External ophthalmoplegia(parent)

Myopathy with cytoplasmic inclusions(parent)

Hereditary disorder of nervous system(parent)

Hereditary disorder of the visual system(parent)

Inherited arthrogryposis(parent)

Myopathy of extraocular muscles(parent)

Quick Facts

SNOMED CT: 724349009
UMLS CUI: C4510610
Fully Specified Name: Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (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.