Human Phenotype Ontology 
Grandparent Node:
expandAbnormal ventricular septum morphology (HP:0010438)help
Parent Node:
expandVentricular septal defect (HP:0001629)help
..Starting node
..expandRestrictive ventricular septal defect (HP:0011683)help
Term ID: 11683
Name: Restrictive ventricular septal defect
Synonym:
Definition: Any ventricular septal defect (VSD) that is small enough to restrict flow across it such that a pressure gradient exists between the two sides of the VSD.
Comments:
Reference: HP:0011683
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandGerbode ventricular septal defect (HP:0011621) help
..expandInlet ventricular septal defect (HP:0011622) help
..expandMuscular ventricular septal defect (HP:0011623) help
..expandNon-restrictive ventricular septal defect (HP:0011684) help
..expandPerimembranous ventricular septal defect (HP:0011682) help
..expandSubarterial ventricular septal defect (HP:0011681) 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:0011683HP:0011683Restrictive ventricular septal defect0 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.