General Information of Disease (ID: DISH7LPY)

Disease Name Idiopathic interstitial pneumonia
Synonyms IPF; noninfectious pneumonia; idiopathic interstitial pneumonitis; idiopathic fibrosing alveolitis; diffuse idiopathic pulmonary fibrosis; IIp
Definition A class of diffuse lung diseases that typically affect the pulmonary interstitium, although some also have a component affecting the airways (for instance, Cryptogenic organizing pneumonitis).
Disease Hierarchy
DIS8EF3M: Pneumonia
DISBBY0S: Idiopathic disease
DISH7LPY: Idiopathic interstitial pneumonia
Disease Identifiers
MONDO ID
MONDO_0002429
MESH ID
D054988
UMLS CUI
C2350236
MedGen ID
389939
Orphanet ID
98300
SNOMED CT ID
700249006

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
SFTPD TTGLMU7 Strong Biomarker [1]
------------------------------------------------------------------------------------
This Disease Is Related to 11 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
BMP3 OTCTI0UW Limited Altered Expression [2]
MUC21 OTQ8GP5L Limited Biomarker [3]
OVGP1 OTL2W9M5 Limited Biomarker [3]
PI15 OTPJL6ML Limited Biomarker [4]
RTKN2 OTV2AXQM Limited Altered Expression [4]
FAM13A OTZ6GN0Q moderate Genetic Variation [5]
HNRNPD OT5UO1FA Strong Altered Expression [6]
MUC5B OTPW6K5C Strong Biomarker [3]
PARN OTTG4PE3 Strong Biomarker [7]
PCBP2 OTXCN9CG Strong Altered Expression [6]
TIAL1 OTV2KFZH Strong Altered Expression [6]
------------------------------------------------------------------------------------
⏷ Show the Full List of 11 DOT(s)

References

1 Evaluation of the Diagnostic Efficacies of Serological Markers KL-6, SP-A, SP-D, CCL2, and CXCL13 in Idiopathic Interstitial Pneumonia.Respiration. 2019;98(6):534-545. doi: 10.1159/000503689. Epub 2019 Oct 30.
2 Reduced expression of BMP3 contributes to the development of pulmonary fibrosis and predicts the unfavorable prognosis in IIP patients.Oncotarget. 2017 Aug 9;8(46):80531-80544. doi: 10.18632/oncotarget.20083. eCollection 2017 Oct 6.
3 Unique expression profiles of mucin proteins in interstitial pneumonia-associated lung adenocarcinomas.Histol Histopathol. 2019 Nov;34(11):1243-1254. doi: 10.14670/HH-18-114. Epub 2019 Apr 9.
4 Relationship between gene expression and lung function in Idiopathic Interstitial Pneumonias.BMC Genomics. 2015 Oct 26;16:869. doi: 10.1186/s12864-015-2102-3.
5 FAM13A polymorphism as a prognostic factor in patients with idiopathic pulmonary fibrosis.Respir Med. 2017 Feb;123:105-109. doi: 10.1016/j.rmed.2016.12.007. Epub 2016 Dec 22.
6 Expression Profile of Six RNA-Binding Proteins in Pulmonary Sarcoidosis.PLoS One. 2016 Aug 30;11(8):e0161669. doi: 10.1371/journal.pone.0161669. eCollection 2016.
7 Telomere-related lung fibrosis is diagnostically heterogeneous but uniformly progressive.Eur Respir J. 2016 Dec;48(6):1710-1720. doi: 10.1183/13993003.00308-2016. Epub 2016 Aug 18.