Arteriovenous malformation

Symptom Information:

Symptom ID: HPO:0100026
Synonyms:
Arteriovenous hemangioma (disorder) [Orphanet:34780]
Arteriovenous malformation (morphologic abnormality) [Orphanet:34780]
Congenital arteriovenous malformation (disorder) [Orphanet:34780]
Arteriovenous malformation [Orphanet:34780]
Congenital arteriovenous malformation [Orphanet:34780]
Arteriovenous malformation [OMIM:Arteriovenous malformation]
Arteriovenous malformations/vascular malformations (excluding port-wine stains) [Orphanet:34780]
Arteriovenous malformation [MedDRA:10003193]
A-V malformation [MedDRA:10003193]
Arteriovenous anomaly [MedDRA:10003193]
Arteriovenous malformations [MedDRA:10003193]
Arteriovenous malformation (cerebral, spinal, pulmonary, liver) [OMIM:Arteriovenous malformation (cerebral, spinal, pulmonary, liver)]
Arteriovenous malformations [OMIM:Arteriovenous malformations]
Vascular anomaly [MedDRA:10047050]
Vascular malformation [Orphanet:34780]
Congenital vascular malformation (disorder) [Orphanet:34780]
Congenital vascular anomaly (morphologic abnormality) [Orphanet:34780]
Vascular anomaly [Orphanet:34780]
Congenital vascular anomaly [Orphanet:34780]
Vascular anomalies (50% of patients) [OMIM:Vascular anomalies (50% of patients)]
Vascular malformations [OMIM:Vascular malformations]
Quality:
Cross references:
Orphanet:34780 "Arteriovenous malformations/vascular malformations (excluding port-wine stains)" [Orphanet:34780]
OMIM: "Arteriovenous malformation" [OMIM:Arteriovenous malformation]
OMIM: "Arteriovenous malformation (cerebral, spinal, pulmonary, liver)" [OMIM:Arteriovenous malformation (cerebral, spinal, pulmonary, liver)]
OMIM: "Arteriovenous malformations" [OMIM:Arteriovenous malformations]
OMIM: "Vascular anomalies (50% of patients)" [OMIM:Vascular anomalies (50% of patients)]
OMIM: "Vascular malformations" [OMIM:Vascular malformations]
UMLS:C0334533 "Arteriovenous malformation" [Orphanet:34780]
UMLS:C0003857 "Congenital arteriovenous malformation" [Orphanet:34780]
UMLS:C0158570 "Vascular anomaly" [Orphanet:34780]
UMLS:C1961121 "Congenital vascular anomaly" [Orphanet:34780]
Is a (Direct Parents):
MedDRA Vascular malformations and acquired anomalies
Orphanet Structural anomalies of the cardio-circulatory system
HPO         Abnormality of the vasculature
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)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular disorders NEC(MedDRA:10047066)
       Vascular malformations and acquired anomalies(MedDRA:10047091)
          Arteriovenous malformation(HPO:0100026)
Database Frequency: 38 / 7739
Resource:

All diseases associated with this symptom:

ADAMS-OLIVER SYNDROME 1 (OMIM:100300)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Aortic arch anomaly - peculiar facies - intellectual deficit (Orphanet:1110)
Arterial dissection - lentiginosis (Orphanet:1682)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Blue rubber bleb nevus (Orphanet:1059)
CHILD syndrome (Orphanet:139)
CLAPO syndrome (Orphanet:168984)
Capillary malformation - arteriovenous malformation (Orphanet:137667)
Classical homocystinuria (Orphanet:394)
Cobb syndrome (Orphanet:53721)
Currarino triad (Orphanet:1552)
Cutis marmorata telangiectatica congenita (Orphanet:1556)
Double uterus - hemivagina - renal agenesis (Orphanet:3411)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Familial multiple nevi flammei (Orphanet:624)
Fanconi anemia (Orphanet:84)
Hennekam syndrome (Orphanet:2136)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Ito hypomelanosis (Orphanet:435)
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (OMIM:175050)
Lhermitte-Duclos disease (Orphanet:65285)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Mucocutaneous venous malformations (Orphanet:2451)
Mucopolysaccharidosis type 7 (Orphanet:584)
POEMS syndrome (Orphanet:2905)
PTEN hamartoma tumor syndrome (Orphanet:306498)
Pelizaeus-Merzbacher disease (Orphanet:702)
Phakomatosis pigmentovascularis (Orphanet:2875)
Proteus syndrome (Orphanet:744)
Proteus-like syndrome (Orphanet:2969)
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus (Orphanet:137608)
TARP syndrome (Orphanet:2886)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER (OMIM:187300)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 (OMIM:600376)
Tumoral calcinosis (Orphanet:53715)
Von Hippel-Lindau disease (Orphanet:892)
Wyburn-Mason syndrome (Orphanet:53719)