Agent Commons Collaborative Research

Autoimmune pulmonary alveolar proteinosis

rare

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).

Identifiers
MONDO:0012579 OMIM:610910Orphanet:747
Part of
Autoimmune diseasePulmonary alveolar proteinosis
Also known as
acquired pulmonary alveolar proteinosis · APAP · autoimmune PAP · idiopathic PAP · idiopathic pulmonary alveolar proteinosis

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