Pulmonary arteriovenous malformation

Symptom Information:

Symptom ID: HPO:0006548
Synonyms:
Pulmonary arteriovenous malformation (PAVM), especially lower lobes [HPO:0006548]
Pulmonary av malformation [HPO:0006548]
Pulmonary arteriovenous malformation [OMIM:Pulmonary arteriovenous malformation]
Pulmonary arteriovenous malformation (PAVM), especially lower lobes [OMIM:Pulmonary arteriovenous malformation (PAVM), especially lower lobes]
Pulmonary arteriovenous malformation (PAVM) [OMIM:Pulmonary arteriovenous malformation (PAVM)]
Quality:
Cross references:
OMIM: "Pulmonary arteriovenous malformation" [OMIM:Pulmonary arteriovenous malformation]
OMIM: "Pulmonary arteriovenous malformation (PAVM), especially lower lobes" [OMIM:Pulmonary arteriovenous malformation (PAVM), especially lower lobes]
OMIM: "Pulmonary arteriovenous malformation (PAVM)" [OMIM:Pulmonary arteriovenous malformation (PAVM)]
Is a (Direct Parents):
HPO         Arteriovenous malformation
HPO         Abnormality of lung morphology
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of the vasculature(HPO:0002597)
             Arteriovenous malformation(HPO:0100026)
                Pulmonary arteriovenous malformation(HPO:0006548)
       Abnormality of the respiratory system(HPO:0002086)
          Abnormal respiratory system morphology(HPO:0012252)
             Abnormality of lung morphology(HPO:0002088)
                Pulmonary arteriovenous malformation(HPO:0006548)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Hereditary hemorrhagic telangiectasia (Orphanet:774)
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (OMIM:175050)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER (OMIM:187300)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 (OMIM:600376)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4 (OMIM:610655)