Exertional dyspnea

Symptom Information:

Symptom ID: HPO:0002875
Synonyms:
Exertional dyspnea [OMIM:Exertional dyspnea]
Dyspnea, exertional [OMIM:Dyspnea, exertional]
Quality:
Cross references:
OMIM: "Exertional dyspnea" [OMIM:Exertional dyspnea]
OMIM: "Dyspnea, exertional" [OMIM:Dyspnea, exertional]
Is a (Direct Parents):
HPO         Dyspnea
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)
                Respiratory insufficiency(HPO:0002093)
                   Dyspnea(HPO:0002094)
                      Exertional dyspnea(HPO:0002875)
          Functional respiratory abnormality(HPO:0002795)
             Respiratory insufficiency(HPO:0002093)
                Dyspnea(HPO:0002094)
                   Exertional dyspnea(HPO:0002875)
MedDRA:
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)