Arteriovenous malformation
Symptom Information:
Symptom ID: | HPO:0100026 | |||||||||||||||||||||
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 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) |
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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) |