Autoimmune pulmonary alveolar proteinosis

MONDO:0012579

Pulmonary alveolar proteinosis (PAP) is a rare lung disease characterized by the accumulation of a lipoproteinaceous substance in the distal air spaces which positively stains with periodic acid-Schiff (PAS).

Also known as: APAP, Pulmonary Alveolar Proteinosis, autoimmune PAP, iPAP, idiopathic PAP, idiopathic pulmonary alveolar proteinosis, PAP, PAP acquired

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