Hemoptysis
Symptom Information:
Symptom ID: | HPO:0002105 | ||||||||||
Synonyms: |
|
||||||||||
Quality: | |||||||||||
Cross references: |
|
||||||||||
Is a (Direct Parents): |
|
||||||||||
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) Hemoptysis(HPO:0002105) MedDRA: Vascular disorders(MedDRA:10047065) Vascular haemorrhagic disorders(MedDRA:10047075) Haemorrhages NEC(MedDRA:10018987) Hemoptysis(HPO:0002105) |
||||||||||
Database Frequency: | 30 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
Allergic bronchopulmonary aspergillosis | (Orphanet:1164) |
Alveolar echinococcosis | (Orphanet:284) |
Anti-glomerular basement membrane disease | (Orphanet:375) |
Behçet disease | (Orphanet:117) |
Chronic mucocutaneous candidiasis | (Orphanet:1334) |
Cogan syndrome | (Orphanet:1467) |
Cryptogenic organizing pneumonia | (Orphanet:1302) |
Desquamative interstitial pneumonia | (Orphanet:98852) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Hemorrhagic fever - renal syndrome | (Orphanet:340) |
Hereditary hemorrhagic telangiectasia | (Orphanet:774) |
Hodgkin lymphoma | (Orphanet:98293) |
Hodgkin lymphoma, classical | (Orphanet:391) |
Hughes-Stovin syndrome | (Orphanet:228116) |
Hydatidosis | (Orphanet:400) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Idiopathic pulmonary alveolar proteinosis | (Orphanet:747) |
Idiopathic pulmonary hemosiderosis | (Orphanet:99931) |
Legionellosis | (Orphanet:549) |
Lymphangioleiomyomatosis | (Orphanet:538) |
Microscopic polyangiitis | (Orphanet:727) |
PULMONARY HEMOSIDEROSIS | (OMIM:178550) |
Pulmonary arterial hypertension | (Orphanet:182090) |
Pulmonary blastoma | (Orphanet:64741) |
Pulmonary capillary hemangiomatosis | (Orphanet:199241) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Takayasu arteritis | (Orphanet:3287) |
Tracheobronchopathia osteochondroplastica | (Orphanet:3348) |