Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3

disorder

SNOMED 720951008CUI C4303760

Overview

Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 is a disorder.

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

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Mitochondrial cytopathy(parent)

Quick Facts

SNOMED CT: 720951008
UMLS CUI: C4303760
Fully Specified Name: Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (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.