Obstructive lung disease

Symptom Information:

Symptom ID: HPO:0006536
Synonyms:
Lung Diseases, Obstructive [Orphanet:33950]
Obstructive lung disease [OMIM:Obstructive lung disease]
Chronic obstructive pulmonary disease/COPD/obstructive respiratory syndrome [Orphanet:33950]
Obstructive airways disorder [Orphanet:33950]
Obstructive airways disorder [MedDRA:10061877]
Airway obstruction NOS [MedDRA:10061877]
Airway resistance increased [MedDRA:10061877]
Airways obstruction [MedDRA:10061877]
Disease obstructive lung [MedDRA:10061877]
Lung disease obstructive [MedDRA:10061877]
Obstruction lung disease [MedDRA:10061877]
Obstructive airways disorder NOS [MedDRA:10061877]
Respiratory obstruction unspecified [MedDRA:10061877]
Lower airway obstruction [MedDRA:10061877]
Airway obstruction [OMIM:Airway obstruction]
Quality:
Cross references:
Orphanet:33950 "Chronic obstructive pulmonary disease/COPD/obstructive respiratory syndrome" [Orphanet:33950]
OMIM: "Obstructive lung disease" [OMIM:Obstructive lung disease]
OMIM: "Airway obstruction" [OMIM:Airway obstruction]
UMLS:C0600260 "Lung Diseases, Obstructive" [Orphanet:33950]
Is a (Direct Parents):
Orphanet Abnormality of the respiratory system
Orphanet Chronic obstructive pulmonary disease
HPO         Abnormality of lung morphology
MedDRA Bronchospasm and obstruction
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the respiratory system(HPO:0002086)
          Abnormal respiratory system morphology(HPO:0012252)
             Abnormality of lung morphology(HPO:0002088)
                Obstructive lung disease(HPO:0006536)
MedDRA:
Respiratory, thoracic and mediastinal disorders(MedDRA:10038738)
    Bronchial disorders (excl neoplasms)(MedDRA:10006436)
       Bronchospasm and obstruction(MedDRA:10006484)
          Obstructive lung disease(HPO:0006536)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

CILIARY DYSKINESIA WITH EXCESSIVELY LONG CILIA (OMIM:242680)
Fabry disease (Orphanet:324)
Hypoplasminogenemia (Orphanet:722)
Ligneous conjunctivitis (Orphanet:97231)
Lymphoid hypereosinophilic syndrome (Orphanet:314970)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)