Cough

Symptom Information:

Symptom ID: [DEL]MedDRA:10011224
Synonyms:
Complaining of cough (finding) [Orphanet:33400]
Coughing (observable entity) [Orphanet:33400]
Cough (finding) [Orphanet:33400]
Does cough (finding) [Orphanet:33400]
Does cough [Orphanet:33400]
Coughing [Orphanet:33400]
Cough [Orphanet:33400]
Cough [OMIM:Cough]
Coughing [OMIM:Coughing]
HPO:0012735 Cough [cm]
Quality:
Cross references:
Orphanet:33400 "Cough" [Orphanet:33400]
OMIM: "Cough" [OMIM:Cough]
OMIM: "Coughing" [OMIM:Coughing]
UMLS:C0687152 "Does cough" [Orphanet:33400]
UMLS:C0010200 "Coughing" [Orphanet:33400]
Is a (Direct Parents):
Orphanet Abnormality of the respiratory system
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 70 / 7739
Resource:

All diseases associated with this symptom:

Adult pulmonary Langerhans cell histiocytosis (Orphanet:99874)
Allergic bronchopulmonary aspergillosis (Orphanet:1164)
Alveolar echinococcosis (Orphanet:284)
Anisakiasis (Orphanet:1070)
Anti-glomerular basement membrane disease (Orphanet:375)
Antisynthetase syndrome (Orphanet:81)
Autosomal agammaglobulinemia (Orphanet:33110)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Babesiosis (Orphanet:108)
CHOLESTEROL PNEUMONIA (OMIM:215030)
CILIARY DYSKINESIA, PRIMARY, 20 (OMIM:615067)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Cogan syndrome (Orphanet:1467)
Congenital pulmonary lymphangiectasia (Orphanet:2414)
Crimean-Congo hemorrhagic fever (Orphanet:99827)
Cutaneous mastocytosis (Orphanet:66646)
Dermatomyositis (Orphanet:221)
Desquamative interstitial pneumonia (Orphanet:98852)
Diffuse panbronchiolitis (Orphanet:171700)
Drug rash with eosinophilia and systemic symptoms (Orphanet:139402)
Ebola hemorrhagic fever (Orphanet:319218)
Eosinophilic granuloma (Orphanet:99871)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Erdheim-Chester disease (Orphanet:35687)
Esophageal adenocarcinoma (Orphanet:99976)
Esophageal carcinoma (Orphanet:70482)
Esophageal squamous cell carcinoma (Orphanet:99977)
Febrile infection-related epilepsy syndrome (Orphanet:163703)
Gaucher disease type 2 (Orphanet:77260)
Giant cell arteritis (Orphanet:397)
Good syndrome (Orphanet:169105)
Granulomatosis with polyangiitis (Orphanet:900)
Hodgkin lymphoma (Orphanet:98293)
Hodgkin lymphoma, classical (Orphanet:391)
Hughes-Stovin syndrome (Orphanet:228116)
Hydatidosis (Orphanet:400)
Hypocomplementemic urticarial vasculitis (Orphanet:36412)
Hypohidrotic ectodermal dysplasia (Orphanet:238468)
Idiopathic acute eosinophilic pneumonia (Orphanet:724)
Idiopathic pulmonary alveolar proteinosis (Orphanet:747)
Juvenile dermatomyositis (Orphanet:93672)
Lassa fever (Orphanet:99824)
Legionellosis (Orphanet:549)
Lyell syndrome (Orphanet:537)
Lymphangioleiomyomatosis (Orphanet:538)
Majeed syndrome (Orphanet:77297)
Malakoplakia (Orphanet:556)
Marburg hemorrhagic fever (Orphanet:99826)
Mastocytosis (Orphanet:98292)
Mucopolysaccharidosis type 1 (Orphanet:579)
Nipah virus disease (Orphanet:99825)
Polymyositis (Orphanet:732)
Pontiac fever (Orphanet:99748)
Primary familial polycythemia (Orphanet:90042)
Pulmonary blastoma (Orphanet:64741)
Relapsing polychondritis (Orphanet:728)
SARCOIDOSIS, SUSCEPTIBILITY TO, 1 (OMIM:181000)
Scleroderma (Orphanet:801)
Scrub typhus (Orphanet:83317)
Stevens-Johnson syndrome (Orphanet:36426)
Sweet syndrome (Orphanet:3243)
Systemic capillary leak syndrome (Orphanet:188)
Thymic carcinoma (Orphanet:99868)
Thymic epithelial neoplasm (Orphanet:3398)
Thymic tumor (Orphanet:100100)
Thymoma (Orphanet:99867)
Tracheobronchopathia osteochondroplastica (Orphanet:3348)
Typhoid (Orphanet:99745)
Whipple disease (Orphanet:3452)
Yellow nail syndrome (Orphanet:662)