Emphysema
Symptom Information:
Symptom ID: | HPO:0002097 | ||||||||||||||||
Synonyms: |
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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) Emphysema(HPO:0002097) MedDRA: Respiratory, thoracic and mediastinal disorders(MedDRA:10038738) Lower respiratory tract disorders (excl obstruction and infection)(MedDRA:10024967) Parenchymal lung disorders NEC(MedDRA:10033979) Emphysema(HPO:0002097) |
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Database Frequency: | 40 / 7739 | ||||||||||||||||
Resource: |
All diseases associated with this symptom:
Allergic bronchopulmonary aspergillosis | (Orphanet:1164) |
Alpha-1-antitrypsin deficiency | (Orphanet:60) |
Autosomal dominant cerebellar ataxia | (Orphanet:99) |
Autosomal dominant cutis laxa | (Orphanet:90348) |
Autosomal recessive cutis laxa type 1 | (Orphanet:90349) |
Autosomal recessive cutis laxa type 2 | (Orphanet:90350) |
BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION | (OMIM:210050) |
Birt-Hogg-Dube syndrome | (Orphanet:122) |
CUTIS LAXA, AUTOSOMAL DOMINANT 1 | (OMIM:123700) |
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA | (OMIM:219100) |
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB | (OMIM:614437) |
Combined pulmonary fibrosis-emphysema syndrome | (Orphanet:300564) |
Common variable immunodeficiency | (Orphanet:1572) |
Congenital lobar emphysema | (Orphanet:1928) |
Cryptogenic organizing pneumonia | (Orphanet:1302) |
Cutis laxa | (Orphanet:209) |
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies | (Orphanet:221145) |
Cutis laxa-Marfanoid syndrome | (Orphanet:171719) |
Cystic fibrosis - gastritis - megaloblastic anemia | (Orphanet:2575) |
EMPHYSEMA, HEREDITARY PULMONARY | (OMIM:130700) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Ellis Van Creveld syndrome | (Orphanet:289) |
Eosinophilic granuloma | (Orphanet:99871) |
Fabry disease | (Orphanet:324) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Hypophosphatasia | (Orphanet:436) |
Idiopathic pulmonary fibrosis | (Orphanet:2032) |
Immunodeficiency by defective expression of HLA class 1 | (Orphanet:34592) |
LOEYS-DIETZ SYNDROME 4 | (OMIM:614816) |
Leprechaunism | (Orphanet:508) |
Lymphangioleiomyomatosis | (Orphanet:538) |
MEIER-GORLIN SYNDROME 4 | (OMIM:613804) |
Marfan syndrome type 1 | (Orphanet:284963) |
Menkes disease | (Orphanet:565) |
Netherton syndrome | (Orphanet:634) |
Respiratory bronchiolitis - interstitial lung disease | (Orphanet:79127) |
Thymic aplasia | (Orphanet:83471) |
Torticollis - keloids - cryptorchidism - renal dysplasia | (Orphanet:3341) |
Tuberous sclerosis | (Orphanet:805) |