Related Conditions
Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome(child)
Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome(child)
Coenzyme Q2, polyprenyltransferase gene related-coenzyme Q10 deficiency(child)
Recessive hereditary disorder (autosomal)(parent)
Disorder of mitochondrial respiratory chain complexes(parent)
Mitochondrial cytopathy(parent)
Quick Facts
- SNOMED CT
- 724575009
- UMLS CUI
- C1843920
- Fully Specified Name
- Coenzyme Q10 deficiency (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.