Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies

disorder

SNOMED 1208937004CUI C5679913

Overview

Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies is a disorder.

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

Related Conditions

Mitochondrial DNA depletion syndrome encephalomyopathic form(parent)

Quick Facts

SNOMED CT: 1208937004
UMLS CUI: C5679913
Fully Specified Name: Mitochondrial deoxyribonucleic acid depletion syndrome, encephalomyopathic form with variable craniofacial anomalies (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.