acute interstitial pneumonia
Information
- Disease name
- acute interstitial pneumonia
- Disease ID
- DOID:2800
- Description
- "A idiopathic interstitial pneumonia which develops suddenly and is severe. Initially, the lung shows edema, hyaline membranes, and interstitial acute inflammation. Later, it develops loose organizing fibrosis, mostly within alveolar septa and type II pneumocyte hyperplasia. Fever, cough, and difficulty breathing develop over 1 to 2 weeks, typically progressing to acute respiratory failure." [url:http\://www.merck.com/mmhe/sec04/ch050/ch050b.html?qt=idiopathic%20interstitial%20pneumonia&alt=sh, url:https\://www.ncbi.nlm.nih.gov/pubmed/11790668]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:2797
- Cross Reference ID (Disease Ontology)
- GARD:12835
- Cross Reference ID (Disease Ontology)
- ICD10CM:J84.114
- Cross Reference ID (Disease Ontology)
- ICD9CM:516.33
- Cross Reference ID (Disease Ontology)
- NCI:C35806
- Cross Reference ID (Disease Ontology)
- ORDO:79126
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:129459004
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C1279945
- Exact Synonym (Disease Ontology)
- accelerated interstitial pneumonia
- Exact Synonym (Disease Ontology)
- acute interstitial pneumonitis
- Exact Synonym (Disease Ontology)
- AIP
- Exact Synonym (Disease Ontology)
- Hamman-Rich disease
- Exact Synonym (Disease Ontology)
- Hamman-Rich syndrome
- Exact Synonym (Disease Ontology)
- Idiopathic pulmonary fibrosis, acute fatal form
- OrphaNumber from OrphaNet (Orphanet)
- 79126