Human Phenotype Ontology 
Grandparent Node:
expandAbnormal jaw morphology (HP:0030791)help
Parent Node:
expandAbnormality of the maxilla (HP:0000326)help
..Starting node
..expandArteriovenous malformation of the maxilla (HP:0031257)help
Term ID: 31257
Name: Arteriovenous malformation of the maxilla
Synonym:
Definition: An arteriovenous malformation is a disruption of the normal vascular pattern in which arteries or arterioles connect directly to the venous collection system, bypassing any capillary bed. This term refers to an arteriovenous malformation located in the maxilla.
Comments:
Reference: HP:0031257
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of frontal process of maxilla (HP:3000044) help
..expandAbnormality of the premaxilla (HP:0010758) help
..expandAplasia of the maxilla (HP:0010667) help
..expandAplasia/Hypoplasia of the maxilla (HP:0009117) help
..expandAsymmetry of the maxilla (HP:0010755) help
..expandHyperplasia of the maxilla (HP:0430028) help
..expandHypoplasia of the maxilla (HP:0000327) help
..expandNarrow maxilla (HP:0002010) 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:0031257HP:0031257Arteriovenous malformation of the maxilla0 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.