Chronic obstructive pulmonary disease
Symptom Information:
Symptom ID: | HPO:0006510 | ||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) Chronic obstructive pulmonary disease(HPO:0006510) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Bronchial disorders (excl neoplasms)(MedDRA:10006436) Bronchospasm and obstruction(MedDRA:10006484) Chronic obstructive pulmonary disease(HPO:0006510) |
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Database Frequency: | 19 / 7739 | ||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
22q11.2 deletion syndrome | (Orphanet:567) |
Alpha-1-antitrypsin deficiency | (Orphanet:60) |
Alström syndrome | (Orphanet:64) |
Bronchiolitis obliterans with obstructive pulmonary disease | (Orphanet:1303) |
CILIARY DYSKINESIA, PRIMARY, 25 | (OMIM:615482) |
Chronic granulomatous disease | (Orphanet:379) |
Congenital pulmonary lymphangiectasia | (Orphanet:2414) |
EMPHYSEMA, HEREDITARY PULMONARY | (OMIM:130700) |
Eosinophilic granuloma | (Orphanet:99871) |
Fabry disease | (Orphanet:324) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Hurler syndrome | (Orphanet:93473) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Hypoplasminogenemia | (Orphanet:722) |
Ligneous conjunctivitis | (Orphanet:97231) |
PULMONARY DISEASE, CHRONIC OBSTRUCTIVE | (OMIM:606963) |
Scheie syndrome | (Orphanet:93474) |
Sneddon syndrome | (Orphanet:820) |
Wiskott-Aldrich syndrome | (Orphanet:906) |