Human Phenotype Ontology 
Grandparent Node:
expandCardiomyopathy (HP:0001638)help
Parent Node:
expandNoncompaction cardiomyopathy (HP:0012817)help
..Starting node
..expandLeft ventricular noncompaction cardiomyopathy (HP:0011664)help
Term ID: 11664
Name: Left ventricular noncompaction cardiomyopathy
Synonym: Left ventricular non-compaction cardiomyopathy
Definition: Left ventricular non-compaction (LVNC) is characterized by prominent left ventricular trabeculae and deep inter-trabecular recesses. The myocardial wall is often thickened with a thin, compacted epicardial layer and a thickened endocardial layer. In some patients, LVNC is associated with left ventricular dilatation and systolic dysfunction, which can be transient in neonates.
Comments:
Reference: HP:0011664
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBiventricular noncompaction cardiomyopathy (HP:0012818) help
..expandRight ventricular noncompaction cardiomyopathy (HP:0012816) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0011664HP:0011664Left ventricular noncompaction cardiomyopathy0DTNA CL E G H1837604169Left ventricular noncompaction 1604169C1858725OMIM15713057601239
HP:0011664HP:0011664Left ventricular noncompaction cardiomyopathy0MIB1 CL E G H57534615092Left ventricular noncompaction 7615092C3554496OMIM141921086608677
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (2) :DTNA MIB1

Diseases (2) :604169 615092
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.