Hepatic arteriovenous malformation

Symptom Information:

Symptom ID: HPO:0006574
Synonyms:
Liver arteriovenous malformation [HPO:0006574]
Hepatic arteriovenous malformation [OMIM:Hepatic arteriovenous malformation]
Liver arteriovenous malformation [OMIM:Liver arteriovenous malformation]
Hepatic arteriovenous malformation [MedDRA:10019633]
Quality:
Cross references:
OMIM: "Hepatic arteriovenous malformation" [OMIM:Hepatic arteriovenous malformation]
OMIM: "Liver arteriovenous malformation" [OMIM:Liver arteriovenous malformation]
Is a (Direct Parents):
MedDRA Vascular malformations and acquired anomalies
HPO         Arteriovenous malformation
HPO         Abnormality of the hepatic vasculature
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the liver(HPO:0001392)
                Abnormality of the hepatic vasculature(HPO:0006707)
                   Hepatic arteriovenous malformation(HPO:0006574)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of the vasculature(HPO:0002597)
             Arteriovenous malformation(HPO:0100026)
                Hepatic arteriovenous malformation(HPO:0006574)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular disorders NEC(MedDRA:10047066)
       Vascular malformations and acquired anomalies(MedDRA:10047091)
          Hepatic arteriovenous malformation(HPO:0006574)
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Hereditary hemorrhagic telangiectasia (Orphanet:774)
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (OMIM:175050)
Neonatal hemochromatosis (Orphanet:446)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER (OMIM:187300)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 (OMIM:600376)