WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:3770 pulmonary fibrosis Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  An interstitial lung disease that is characterized by destruction, scarring, and thickening of the interstitial lung tissues and progressive pulmonary function loss in a restrictive pattern, has_symptom progressive shortness of breath, fatigue, and chronic cough, possibly has_material_basis_in exposure to certain chemicals, autoimmune conditions, and radiation. It can be caused by inhaling hazardous chemicals, certain diseases, medication and genetics or unknown causes.

1 Ontology

Name
Disease Ontology

9 Parents

Identifier Name Description
DOID:7 disease of anatomical entity A disease that manifests in a defined anatomical structure.
DOID:4 disease A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism.
DOID:0050161 lower respiratory tract disease A respiratory system disease which involves the lower respiratory tract.
DOID:1579 respiratory system disease A disease of anatomical entity that located_in the respiratory system which extends from the nasal sinuses to the diaphragm.
DOID:850 lung disease A lower respiratory tract disease in which the function of the lungs is adversely affected by narrowing or blockage of the airways resulting in poor air flow, a loss of elasticity in the lungs that produces a decrease in the total volume of air that the lungs are able to hold, and clotting, scarring, or inflammation of the blood vessels that affect the ability of the lungs to take up oxygen and to release carbon dioxide.
DOID:17 musculoskeletal system disease A disease of anatomical entity that occurs in the muscular and/or skeletal system.
DOID:65 connective tissue disease A musculoskeletal system disease that affects tissues such as skin, tendons, and cartilage.
DOID:3770 pulmonary fibrosis An interstitial lung disease that is characterized by destruction, scarring, and thickening of the interstitial lung tissues and progressive pulmonary function loss in a restrictive pattern, has_symptom progressive shortness of breath, fatigue, and chronic cough, possibly has_material_basis_in exposure to certain chemicals, autoimmune conditions, and radiation. It can be caused by inhaling hazardous chemicals, certain diseases, medication and genetics or unknown causes.
DOID:3082 interstitial lung disease A lung disease that is characterized by inflammation and altered lung interstitium compromising pulmonary function and often has_symptom shortness of breath, dyspnea, and/or cough.

12 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:3770 DOID:0050156
is_a DOID:3770 DOID:12123
is_a DOID:3082 DOID:3770
is_a DOID:4 DOID:3770
is_a DOID:65 DOID:3770
is_a DOID:850 DOID:3770
is_a DOID:1579 DOID:3770
is_a DOID:7 DOID:3770
is_a DOID:0050161 DOID:3770
is_a DOID:17 DOID:3770
is_a DOID:3770 DOID:5641
is_a DOID:3770 DOID:5642

1 Synonyms

Name Type
Fibrosis of lung synonym