noncompaction cardiomyopathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of cardiomyopathy characterized anatomically by deep trabeculations in the ventricular wall, which define recesses communicating with the main ventricular chamber. (Human Phenotype Ontology, HP_0012817)
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1 genes associated with the noncompaction cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DNAJC19 DnaJ (Hsp40) homolog, subfamily C, member 19