|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the noncompaction cardiomyopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|DNAJC19||DnaJ (Hsp40) homolog, subfamily C, member 19|