Overview
Hypertrophic mitochondrial cardiomyopathy is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Hypertrophic mitochondrial cardiomyopathy associated with cataracts and lactic acidosis(child)
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome(child)
Sengers syndrome(child)
Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency(child)
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial deoxyribonucleic acid mutation(child)
COXPD10 - combined oxidative phosphorylation defect type 10(child)
COXPD17 - combined oxidative phosphorylation defect type 17(child)
Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome(child)
Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome(child)
QRSL1-related combined oxidative phosphorylation defect(child)
Mitochondrial cardiomyopathy(parent)
Hypertrophic cardiomyopathy due to disorder(parent)
Quick Facts
- SNOMED CT
- 472316006
- UMLS CUI
- C3532240
- Fully Specified Name
- Hypertrophic mitochondrial cardiomyopathy (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.