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Gastrointestinal arteriovenous malformation

Symptom ID:

HPO:0002629

Synonyms:

Gastrointestinal arteriovenous malformation [MedDRA:10017932]

Quality:

Cross references:

Is a (Direct Parents):

HPO	Arteriovenous malformation
MedDRA	Vascular malformations and acquired anomalies
HPO	Abnormality of gastrointestinal 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)
                Gastrointestinal arteriovenous malformation(HPO:0002629)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the gastrointestinal tract(HPO:0011024)
                Abnormality of gastrointestinal vasculature(HPO:0004296)
                   Gastrointestinal arteriovenous malformation(HPO:0002629)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular disorders NEC(MedDRA:10047066)
       Vascular malformations and acquired anomalies(MedDRA:10047091)
          Gastrointestinal arteriovenous malformation(HPO:0002629)

Database Frequency:

2 / 7739

Resource:

Hereditary hemorrhagic telangiectasia	(Orphanet:774)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2	(OMIM:600376)

	Field	Query
	Disease
	Symptom