Exertional dyspnea
Symptom Information:
Symptom ID: | HPO:0002875 | ||
Synonyms: |
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Quality: | |||
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) Functional respiratory abnormality(HPO:0002795) Respiratory insufficiency(HPO:0002093) Dyspnea(HPO:0002094) Exertional dyspnea(HPO:0002875) Abnormal respiratory system morphology(HPO:0012252) Abnormality of lung morphology(HPO:0002088) Respiratory insufficiency(HPO:0002093) Dyspnea(HPO:0002094) Exertional dyspnea(HPO:0002875) MedDRA: |
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Database Frequency: | 29 / 7739 | ||
Resource: |
All diseases associated with this symptom:
AREDYLD syndrome | (Orphanet:1133) |
ATTRV122I amyloidosis | (Orphanet:85451) |
Acute interstitial pneumonia | (Orphanet:79126) |
Autosomal dominant limb-girdle muscular dystrophy type 1B | (Orphanet:264) |
Cardiomyopathy, familial restrictive 2 | (OMIM:609578) |
Combined pulmonary fibrosis-emphysema syndrome | (Orphanet:300564) |
Familial atrial myxoma | (Orphanet:615) |
Familial isolated hypertrophic cardiomyopathy | (Orphanet:155) |
Gaucher disease - ophthalmoplegia - cardiovascular calcification | (Orphanet:2072) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hermansky-Pudlak syndrome | (Orphanet:79430) |
Hermansky-Pudlak syndrome with pulmonary fibrosis | (Orphanet:231500) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Idiopathic pulmonary fibrosis | (Orphanet:2032) |
Isolated cytochrome C oxidase deficiency | (Orphanet:254905) |
LMNA-related cardiocutaneous progeria syndrome | (Orphanet:363618) |
Loeffler endocarditis | (Orphanet:75566) |
Lymphoid interstitial pneumonia | (Orphanet:79128) |
Mitochondrial DNA deletion syndrome with progressive myopathy | (Orphanet:352470) |
Mulibrey nanism | (Orphanet:2576) |
PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:265400) |
Primary familial polycythemia | (Orphanet:90042) |
Recessive hereditary methemoglobinemia type 1 | (Orphanet:139373) |
Recessive hereditary methemoglobinemia type 2 | (Orphanet:139380) |
Respiratory bronchiolitis - interstitial lung disease | (Orphanet:79127) |
X-linked Emery-Dreifuss muscular dystrophy | (Orphanet:98863) |