Mitochondrial respiratory chain complex I assembly gene defect

disorder

SNOMED 1196948002CUI C5686079

Overview

Mitochondrial respiratory chain complex I assembly gene defect is a disorder.

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

Related Conditions

Mitochondrial complex I deficiency nuclear type 10(child)

Nicotinamide adenine dinucleotide coenzyme Q reductase deficiency(parent)

Encephalomyeloneuropathy(parent)

Quick Facts

SNOMED CT: 1196948002
UMLS CUI: C5686079
Fully Specified Name: Mitochondrial respiratory chain complex I assembly gene defect (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.