interstitial lung disease 2
Information
- Disease name
- interstitial lung disease 2
- Disease ID
- DOID:0050156
- Description
- "An interstitial lung disease pulmonary fibrosis that is characterized by scarring of the lung and that has_material_basis_in heterozygous mutation in the SFTPA2 gene on chromosome 10q22." [url:https\://pubmed.ncbi.nlm.nih.gov/32855221/, url:https\://www.pulmonaryfibrosis.org/life-with-pf/about-ipf]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:3082
- Cross Reference ID (Disease Ontology)
- EFO:0000768
- Cross Reference ID (Disease Ontology)
- GARD:8609
- Cross Reference ID (Disease Ontology)
- ICD10CM:J84.112
- Cross Reference ID (Disease Ontology)
- ICD9CM:516.31
- Cross Reference ID (Disease Ontology)
- MESH:D054990
- Cross Reference ID (Disease Ontology)
- MIM:178500
- Cross Reference ID (Disease Ontology)
- NCI:C35716
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:28168000
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C1800706
- Exact Synonym (Disease Ontology)
- cryptogenic fibrosing alveolitis
- Exact Synonym (Disease Ontology)
- FIBROCYSTIC PULMONARY DYSPLASIA
- Exact Synonym (Disease Ontology)
- idiopathic pulmonary fibrosis
- Exact Synonym (Disease Ontology)
- IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL