Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder)
| Code | 766883006 |
|---|---|
| Semantic tag | disorder |
| Module | international |
| Definition | primitive |
| Effective time | 20180731 |
11164009Autosomal dominant hereditary disorder
disorder
363005004Cardiovascular system hereditary disorder
disorder
44808001Conduction disorder of the heart
disorder
399020009Dilated cardiomyopathy
disorder
35728003Familial cardiomyopathy
disorder
None (leaf concept).