Human Phenotype Ontology 
Grandparent Node:
expandCongenital malformation of the right heart (HP:0011723)help
Grandparent Node:
expandConotruncal defect (HP:0001710)help
Parent Node:
expandDouble outlet right ventricle (HP:0001719)help
..Starting node
..expandDouble outlet right ventricle with non-committed ventricular septal defect and pulmonary stenosis (HP:0011653)help
Term ID: 11653
Name: Double outlet right ventricle with non-committed ventricular septal defect and pulmonary stenosis
Synonym: DORV with non-committed VSD and pulmonary stenosis
Definition: A double outlet right ventricle with a non-committed ventricular septal defect (VSD), which is a VSD that is anatomically related to, or close to, neither great vessel, being separated from both by considerable muscle, and also has a pulmonary stenosis; abnormal narrowing or constriction of the pulmonary artery, in the main pulmonary artery and/or in the left or right pulmonary artery branches.
Comments:
Reference: HP:0011653
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDouble outlet right ventricle with doubly committed ventricular septal defect and pulmonary stenosis (HP:0011651) help
..expandDouble outlet right ventricle with doubly committed ventricular septal defect without pulmonary stenosis (HP:0011652) help
..expandDouble outlet right ventricle with non-committed ventricular septal defect without pulmonary stenosis (HP:0011654) help
..expandDouble outlet right ventricle with subaortic ventricular septal defect and pulmonary stenosis (HP:0011655) help
..expandDouble outlet right ventricle with subaortic ventricular septal defect without pulmonary stenosis (HP:0011656) help
..expandDouble outlet right ventricle with subpulmonary ventricular septal defect and pulmonary stenosis (HP:0011657) help
..expandDouble outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis (HP:0011658) 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:0011653HP:0011653Double outlet right ventricle with non-committed ventricular septal defect and pulmonary stenosis0 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.