dilated cardiomyopathy 1E
Also known as CDCD2, CMD1E, SCN5A familial isolated dilated cardiomyopathy, cardiomyopathy dilated with conduction defect type 2+8 more
CDCD2, CMD1E, SCN5A familial isolated dilated cardiomyopathy, cardiomyopathy dilated with conduction defect type 2, cardiomyopathy, dilated, 1E, cardiomyopathy, dilated, type 1E, cardiomyopathy, dilated, with conduction defect 2, cardiomyopathy, dilated, with conduction disorder and arrhythmia, dilated cardiomyopathy type 1E, dilated cardiomyopathy with conduction defect 2, dilated cardiomyopathy with conduction disorder and arrhythmia, familial isolated dilated cardiomyopathy caused by mutation in SCN5A.
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An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
CDCD2, CMD1E, SCN5A familial isolated dilated cardiomyopathy, cardiomyopathy dilated with conduction defect type 2, cardiomyopathy, dilated, 1E, cardiomyopathy, dilated, type 1E, cardiomyopathy, dilated, with conduction defect 2, cardiomyopathy, dilated, with conduction disorder and arrhythmia, dilated cardiomyopathy type 1E, dilated cardiomyopathy with conduction defect 2, dilated cardiomyopathy with conduction disorder and arrhythmia, familial isolated dilated cardiomyopathy caused by mutation in SCN5A
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.