Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder) | | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | | Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation
| | A rare familial dilated cardiomyopathy with characteristics of left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy and elevated serum creatine kinase. | | familiaire gedilateerde cardiomyopathie met geleidingsdefect door mutatie in LMNA-gen | | familiaire gedilateerde cardiomyopathie met geleidingsdefect door LMNA-mutatie familiaire gedilateerde cardiomyopathie met geleidingsdefect door mutatie van lamin A/C
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| Id | 766883006 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
ICD-10 complex map reference set | Target | I42.0 | Rule | TRUE | Advice | ALWAYS I42.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | Correlation | SNOMED CT source code to target map code correlation not specified |
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