| Disease ID | Source | Name | Description |
| 601493 | OMIM | Cardiomyopathy, dilated 1C, with or without left ventricular non-compaction (CMD1C) | A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. Cardiomyopathy dilated type 1C is associated with left ventricular non-compaction in some patients. Left ventricular non-compaction is characterized by numerous prominent trabeculations and deep intertrabecular recesses in hypertrophied and hypokinetic segments of the left ventricle. The disease is caused by variants affecting the gene represented in this entry. |
| 601493 | OMIM | Cardiomyopathy, dilated 1C, with or without left ventricular non-compaction (CMD1C) | A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. Cardiomyopathy dilated type 1C is associated with left ventricular non-compaction in some patients. Left ventricular non-compaction is characterized by numerous prominent trabeculations and deep intertrabecular recesses in hypertrophied and hypokinetic segments of the left ventricle. The disease is caused by variants affecting the gene represented in this entry. |
| 609452 | OMIM | Myopathy, myofibrillar, 4 (MFM4) | A form of myofibrillar myopathy, a group of chronic neuromuscular disorders characterized at ultrastructural level by disintegration of the sarcomeric Z disk and myofibrils, and replacement of the normal myofibrillar markings by small dense granules, or larger hyaline masses, or amorphous material. MFM4 is characterized by distal and proximal muscle weakness with signs of cardiomyopathy and neuropathy. The disease is caused by variants affecting the gene represented in this entry. |