|
| General Information | |||
|---|---|---|---|
| Term | interstitial lung disease 1 | ID (Ontology) | DOID:0060941 (Human Disease) |
| Definition | An interstitial lung disease characterized by a progressive remodeling of the alveolar interstitium that has_material_basis_in heterozygous mutation in the SFTPA1 gene on chromosome 10q22. | ||
| Also Known As | "Idiopathic pulmonary fibrosis" | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
autosomal genetic disease |__autosomal dominant disease___ |__autosomal recessive disease__| connective tissue disease | |__interstitial lung disease____| lung disease | |__interstitial lung disease____| interstitial lung disease 1 |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a |
autosomal dominant disease autosomal recessive disease interstitial lung disease |
||
| Part of | |||
|
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
|
External Crossreferences & Linkouts
|
|||
|
GARD:8609 MIM:619611 ORDO:2032 |
|||