Human Phenotype Ontology 
Grandparent Node:
expandAbnormal vascular morphology (HP:0025015)help
Parent Node:
expandArteriovenous malformation (HP:0100026)help
..Starting node
..expandUterine arteriovenous malformation (HP:0031347)help
Term ID: 31347
Name: Uterine 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 uterus.
Comments:
Reference: HP:0031347
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandArteriovenous fistula (HP:0004947) help
..expandCerebral arteriovenous malformation (HP:0002408) help
..expandGastrointestinal arteriovenous malformation (HP:0002629) help
..expandHepatic arteriovenous malformation (HP:0006574) help
..expandPelvic arteriovenous malformation (HP:0031344) help
..expandPulmonary arteriovenous malformation (HP:0006548) help
..expandSpinal arteriovenous malformation (HP:0002390) 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:0031347HP:0031347Uterine 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.