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Multiple mitochondrial dysfunctions syndrome
disorderSNOMED 720827002CUI C3502075
Overview
By MedlinePlus, National Library of Medicine
Courtesy of the National Library of Medicine. Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.
Related Conditions
MMDS1 - multiple mitochondrial dysfunctions syndrome type 1(child)
Multiple mitochondrial dysfunctions syndrome type 2(child)
Multiple mitochondrial dysfunctions syndrome type 3(child)
Multiple mitochondrial dysfunctions syndrome type 4(child)
ISCA1 deficiency(child)
PMPCB (peptidase mitochondrial processing subunit beta) deficiency(child)
Recessive hereditary disorder (autosomal)(parent)
Disorder of mitochondrial respiratory chain complexes(parent)
Quick Facts
- SNOMED CT
- 720827002
- UMLS CUI
- C3502075
- Fully Specified Name
- Multiple mitochondrial dysfunctions syndrome (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.