Overview
Peroxisome biogenesis disorder spectrum is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Zellweger syndrome(child)
Neonatal adrenoleucodystrophy(child)
Infantile Refsum's disease(child)
PEX5 deficiency(child)
PEX6 deficiency(child)
PEX1 deficiency(child)
PEX10 deficiency(child)
PEX13 deficiency(child)
PEX12 deficiency(child)
PEX16 deficiency(child)
PEX14 deficiency(child)
PEX26 deficiency(child)
PEX3 deficiency(child)
PEX19 deficiency(child)
PEX2 deficiency(child)
Deafness, enamel hypoplasia, nail defect syndrome(child)
Recessive hereditary disorder (autosomal)(parent)
Disorder of peroxisomal function(parent)
Quick Facts
- SNOMED CT
- 742876007
- UMLS CUI
- C3658299
- Fully Specified Name
- Peroxisome biogenesis disorder (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.