Overview
Loss of single peroxisomal function is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Peroxisomal thiolase deficiency(child)
Bifunctional peroxisomal enzyme deficiency(child)
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Isolated DHAP-AT - dihydroxyacetone phosphate acyltransferase deficiency(child)
Isolated alkyldihydroxyacetone phosphate synthase deficiency(child)
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Primary hyperoxaluria, type I(child)
Acatalasemia(child)
Leukoencephalopathy, dystonia, motor neuropathy syndrome(child)
Contiguous ABCD1 DXS1357E deletion syndrome(child)
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FAR1 deficiency(child)
Disorder of peroxisomal function(parent)
Quick Facts
- SNOMED CT
- 238066006
- UMLS CUI
- C0751710
- Fully Specified Name
- Loss of single peroxisomal function (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.