Cerebral arteriovenous malformation
Symptom Information:
Symptom ID: | HPO:0002408 | ||||
Synonyms: |
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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) Cerebral arteriovenous malformation(HPO:0002408) MedDRA: |
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Database Frequency: | 7 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Cerebral arteriovenous malformation | (Orphanet:46724) |
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) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4 | (OMIM:610655) |