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 left ventricle (HP:0011555)help
Term ID: 11555
Name: Double inlet left ventricle
Synonym:
Definition: The condition in which both atria are joined to the left ventricle each by its own atrioventricular valve. Usually there is a hypoplastic right ventricle, which may be on the opposite side of the heart as usual.
Comments:
Reference: HP:0011555
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDouble inlet right ventricle (HP:0011556) 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:0011555HP:0011555Double inlet left ventricle0MAPKAPK5 CL E G H85506889OMIM:619869
HP:0011555HP:0011555Double inlet left ventricle0NODAL CL E G H48387865OMIM:270100Heterotaxy, visceral, 545
HP:0011555HP:0011555Double inlet left ventricle0PLD1 CL E G H53379067OMIM:212093Cardiac valvular defect, developmental4


Genes (3) :MAPKAPK5 NODAL PLD1

Diseases (3) :OMIM:619869 OMIM:270100 OMIM:212093
 

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