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hereditary pulmonary alveolar proteinosis

Disease Summary
Associated Targets (6)
Tbio

3

Tclin

2

Tchem

1


GARD Rare
Mondo Description Congenital pulmonary alveolar proteinosis is a very rare primary interstitial lung disease due to pulmonary surfactant accumulation within the alveolar macrophages and alveoli, characterized by a variable clinical course ranging from an asymptomatic clinical presentation and spontaneous remission, to symptoms such as dyspnea and cough, or to severe respiratory failure.
Mondo Term and Equivalent IDs
MONDO:0012580:  hereditary pulmonary alveolar proteinosis
GARD:0004582: 
MESH:C535832: 
OMIMPS:265120: 
Orphanet:264675: 
SCTID:707442002: 
UMLS:C2931035: