Acute Interstitial Pneumonia
Disease ID: disease_node_14548
Connections displayed (default: 10).
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| Dbxref | GARD:12835, ICD10CM:J84.114, ICD9CM:516.33, NCI:C35806, ORDO:79126, SNOMEDCT_US_2023_03_01:129459004, UMLS_CUI:C1279945 |
|---|---|
| Subclassof | DOID_2797 |
| Data Source | DOID |
| Synonyms | AIP, Hamman-Rich disease, Hamman-Rich syndrome, Idiopathic pulmonary fibrosis, acute fatal form, accelerated interstitial pneumonia, acute interstitial pneumonitis |
| Doid Label | acute interstitial pneumonia |
| Doid 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. |
| Has Symptom | SYMP_0000614 |
| Disease Node Id | disease_node_14548 |
| Doid Id | DOID_2800 |
| Label | Acute Interstitial Pneumonia |
- Outgoing r'ship
HAS_SYMPTOMto/from Cough(ID:disease_node_2282;disease_node_21170) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Hamman-Rich Syndrome(ID:disease_node_418) (Disease)