Emphysema

Symptom Information:

Symptom ID: HPO:0002097
Synonyms:
Pulmonary emphysema [HPO:0002097]
Lung emphysema [Orphanet:33250]
Emphysema (morphologic abnormality) [Orphanet:33250]
Pulmonary emphysema (disorder) [Orphanet:33250]
Pulmonary Emphysema [Orphanet:33250]
Emphysema [OMIM:Emphysema]
Emphysema [Orphanet:33250]
Emphysema [MedDRA:10014561]
Compensatory emphysema [MedDRA:10014561]
Emphysema pulmonary [MedDRA:10014561]
Interstitial emphysema [MedDRA:10014561]
Interstitial emphysema and related conditions of newborn [MedDRA:10014561]
Other emphysema [MedDRA:10014561]
Centrilobular emphysema [MedDRA:10014561]
Paraseptal emphysema [MedDRA:10014561]
Emphysema (rare) [OMIM:Emphysema (rare)]
Quality:
Cross references:
Orphanet:33250 "Emphysema" [Orphanet:33250]
OMIM: "Emphysema" [OMIM:Emphysema]
OMIM: "Emphysema (rare)" [OMIM:Emphysema (rare)]
UMLS:C0034067 "Emphysema" [HPO:0002097]
UMLS:C0034067 "Pulmonary Emphysema" [Orphanet:33250]
Is a (Direct Parents):
MedDRA Parenchymal lung disorders NEC
Orphanet Abnormality of the respiratory system
HPO         Abnormality of lung morphology
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)
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)