Human Phenotype Ontology 
Grandparent Node:
expandAbnormal gastrointestinal vascular morphology (HP:0004296)help
Grandparent Node:
expandArteriovenous malformation (HP:0100026)help
Parent Node:
expandGastrointestinal arteriovenous malformation (HP:0002629)help
..Starting node
..expandDuodenal arteriovenous malformation (HP:0031342)help
Term ID: 31342
Name: Duodenal arteriovenous malformation
Synonym:
Definition: An anomalous configuration of blood vessels that shunts arterial blood directly into veins without passing through the capillaries and that is located in the duodenum.
Comments:
Reference: HP:0031342
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandColonic arteriovenous malformation (HP:0031345) help
..expandGastric arteriovenous malformation (HP:0031341) help
..expandJejunal arteriovenous malformation (HP:0031343) help
..expandRectal arteriovenous malformation (HP:0031346) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031342HP:0031342Duodenal arteriovenous malformation0 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.