Related Conditions
Secondary pulmonary alveolar proteinosis(child)
Autoimmune pulmonary alveolar proteinosis(child)
Congenital pulmonary alveolar proteinosis(child)
2'-5'-oligoadenylate synthetase 1-related infantile-onset pulmonary alveolar proteinosis, hypogammaglobulinaemia(child)
Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency(child)
Proteinosis(parent)
Alveolar pneumopathy(parent)
Quick Facts
- SNOMED CT
- 10501004
- UMLS CUI
- C0034050
- Fully Specified Name
- Pulmonary alveolar proteinosis (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.