Human Phenotype Ontology 
Grandparent Node:
expandAbnormal cardiac ventricle morphology (HP:0001713)help
Parent Node:
expandDouble inlet atrioventricular connection (HP:0011554)help
Parent Node:
expandSingle ventricle (HP:0001750)help
..Starting node
..expandDouble inlet right ventricle (HP:0011556)help
Term ID: 11556
Name: Double inlet right ventricle
Synonym:
Definition: The condition in which both atria are joined to the right ventricle each by its own atrioventricular valve. Usually, the left ventricle is hypoplastic.
Comments:
Reference: HP:0011556
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDouble inlet left ventricle (HP:0011555) help
..expandDouble inlet to single ventricle of indeterminate morphology (HP:0011557) help
..expandSingle ventricle of indeterminate morphology (HP:0011680) 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:0011556HP:0011556Double inlet right ventricle0CIROP CL E G H10012890853647OMIM:619702HETEROTAXY, VISCERAL, 12, AUTOSOMAL; HTX12


Genes (1) :CIROP

Diseases (1) :OMIM:619702
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.