| 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) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0012817 |
| Similar Terms | |
| 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.
| Symbol | Name |
|---|---|
| DNAJC19 | DnaJ (Hsp40) homolog, subfamily C, member 19 |
