Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the cardiovascular system (HP:0001626)help
Parent Node:
expandAbnormal fetal cardiovascular morphology (HP:0010948)help
..Starting node
..expandCongenital portosystemic venous shunt (HP:0012022)help
Term ID: 12022
Name: Congenital portosystemic venous shunt
Synonym:
Definition: A congenital defect of the vasculature such that there is a shunt (by-pass) of blood directly from the portal vein to the vena cava (i.e., the blood from the portal vein is not filtered through the liver).
Comments:
Reference: HP:0012022
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of ductus venosus blood flow (HP:0010947) help
..expandAbnormality of umbilical vein blood flow (HP:0010949) help
..expandEchogenic intracardiac focus (HP:0010942) help
..expandPersistent fetal circulation (HP:0011726) help
..expandPersistent patent ductus venosus (HP:0012021) help
..expandSingle umbilical artery (HP:0001195) 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:0012022HP:0012022Congenital portosystemic venous shunt0 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.