Interstitial Pneumonitis, Desquamative, Familial (DIP)

Alias:
Desquamative Interstitial Pneumonia
Respiratory Bronchiolitis-Associated Interstitial Lung Disease
Respiratory Bronchiolitis Associated Interstitial Lung Disease
Pneumonitis, Desquamative Interstitial, Familial
Pneumonia, Desquamative Interstitial, Familial
Familial Desquamative Interstitial Pneumonitis
Interstitial Lung Disease, Desquamative
Ild, Desquamative
Rbild
Dip
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Interstitial Pneumonitis, Desquamative, Familial, also known as desquamative interstitial pneumonia, is related to pulmonary alveolar proteinosis and bronchopulmonary dysplasia, and has symptoms including coughing, cyanosis and respiratory distress. An important gene associated with Interstitial Pneumonitis, Desquamative, Familial is SFTPC (Surfactant Protein C), and among its related pathways/superpathways are Metabolism of proteins and Diseases of glycosylation. Affiliated tissues include lung and lymph node, and related phenotypes are failure to thrive and recurrent upper respiratory tract infections
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
14
90
12

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

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CAS Number
Status
Phase
No data available

Disease Model

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

References Literature

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PMID
Journal
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IF
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