← Back to Conditions
Disorder of mitochondrial respiratory chain complexes
disorderSNOMED 237986005CUI C0342774
Overview
Disorder of mitochondrial respiratory chain complexes is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Deficiency in enzyme complexes of mitochondrial respiratory chain(child)
Deletion and duplication of mitochondrial DNA(child)
Depletion of mitochondrial DNA(child)
Multiple mitochondrial dysfunctions syndrome(child)
Acyl-CoA dehydrogenase 9 deficiency(child)
Lethal infantile mitochondrial myopathy(child)
Growth and developmental delay, hypotonia, vision impairment, lactic acidosis syndrome(child)
Mitochondrial DNA deletion syndrome with limb-girdle weakness(child)
MEGDEL syndrome(child)
Severe X-linked mitochondrial encephalomyopathy(child)
Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome(child)
Combined oxidative phosphorylation defect type 30(child)
Combined oxidative phosphorylation defect type 29(child)
Combined oxidative phosphorylation defect type 27(child)
Combined oxidative phosphorylation defect type 26(child)
Combined oxidative phosphorylation defect type 23(child)
QRSL1-related combined oxidative phosphorylation defect(child)
Syndromic sensorineural hearing loss due to COXPD (combined oxidative phosphorylation defect)(child)
Renal tubulopathy with encephalopathy and liver failure syndrome(child)
Coenzyme Q10 deficiency(child)
Quick Facts
- SNOMED CT
- 237986005
- UMLS CUI
- C0342774
- Fully Specified Name
- Disorder of mitochondrial respiratory chain complexes (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.