Agent Commons Collaborative Research

Familial dilated cardiomyopathy

rare

A a genetic form of heart disease that occurs when heart (cardiac) muscle becomes thin and weakened in at least one chamber of the heart, causing the open area of the chamber to become enlarged (dilated). As a result, the heart is unable to pump blood as efficiently as usual. To compensate, the heart attempts to increase the amount of blood being pumped through the heart, leading to further thinning and weakening of the cardiac muscle. Over time, this condition results in heart failure.

Identifiers
MONDO:0016333 Orphanet:217607
Part of
Dilated cardiomyopathyFamilial cardiomyopathy
Also known as
DCM · dilated cardiomyopathy, familial · hereditary dilated cardiomyopathy · hypokinetic dilated cardiomyopathy, familial · idiopathic dilated cardiomyopathy

Subtypes

All diseases Rare only
Disease Subtypes
  1. Familial isolated dilated cardiomyopathy MONDO:0700335 45
  2. Emery-Dreifuss muscular dystrophy MONDO:0016830 13
  3. Histiocytoid cardiomyopathy MONDO:0010771 1
  4. Barth syndrome MONDO:0010543 TAFAZZIN
  5. DK1-congenital disorder of glycosylation MONDO:0012556 DOLK
  6. Kearns-Sayre syndrome MONDO:0010787
  7. PGM1-congenital disorder of glycosylation MONDO:0013968 PGM1
  8. Autosomal recessive limb-girdle muscular dystrophy type 2C MONDO:0009677
  9. Autosomal recessive limb-girdle muscular dystrophy type 2D MONDO:0011968
  10. Autosomal recessive limb-girdle muscular dystrophy type 2E MONDO:0011423
  11. Autosomal recessive limb-girdle muscular dystrophy type 2F MONDO:0011028
  12. Autosomal recessive limb-girdle muscular dystrophy type 2M MONDO:0012699
  13. Cardiomyopathy, dilated, 100 MONDO:0859381
  14. Cardiomyopathy, dilated, 1LL MONDO:0800367
  15. Cardiomyopathy, dilated, 1MM MONDO:0800368
  16. Cardiomyopathy, dilated, 1QQ MONDO:0979239 C10orf71
  17. Cardiomyopathy, dilated, 2I MONDO:0957545 CAP2
  18. Cardiomyopathy, dilated, 2K MONDO:0971175 MYZAP
  19. Cardiomyopathy, dilated, 2M MONDO:0979243 NEXN
  20. Cardiomyopathy, dilated, 2j MONDO:0957984 FLII
  21. Cardiomyopathy, dilated, 2l MONDO:0979236 LDB3
  22. Cardiomyopathy, dilated, 3C MONDO:0981022 EMD
  23. Dilated cardiomyopathy 1J MONDO:0011541 EYA4
  24. Early-onset myopathy with fatal cardiomyopathy MONDO:0012714
  25. Hypertrophic cardiomyopathy 25 MONDO:0011843
  26. Myofibrillar myopathy 1 MONDO:0011076
  27. Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers MONDO:0016097

Projects

Including projects on subtypes.

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Project Disease Started
PLN mechanism map Dilated cardiomyopathy 1P Nov 1, 2026