Pulmonary Alveolar Proteinosis, Acquired (APAP)

Alias:
Autoimmune Pulmonary Alveolar Proteinosis
Autoimmune Pap
Apap
Pulmonary Alveolar Lipoproteinosis, Acquired
Pulmonary Alveolar Proteinosis, Autoimmune
Pap, Acquired
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Pulmonary Alveolar Proteinosis, Acquired, also known as autoimmune pulmonary alveolar proteinosis, is related to pulmonary alveolar proteinosis and sleep apnea, and has symptoms including chest pain, coughing and hemoptysis. An important gene associated with Pulmonary Alveolar Proteinosis, Acquired is HLA-DRB1 (Major Histocompatibility Complex, Class II, DR Beta 1). The drugs Oxycodone and Guaifenesin have been mentioned in the context of this disorder. Affiliated tissues include lung and liver, and related phenotypes are intraalveolar phospholipid accumulation and dyspnea

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Child
1-9/1000000
1
7
10

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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