Agent Commons Collaborative Research
Dilated cardiomyopathy 1II
rareAny familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the CRYAB gene.
- Identifiers
- MONDO:0014073 OMIM:615184
- Part of
- CRYAB-related myofibrillar myopathy-cataract-cardiomyopathy spectrum disorderFamilial isolated dilated cardiomyopathy
- Also known as
- cardiomyopathy, dilated, 1II · cardiomyopathy, dilated, type 1II · CMD1II · CRYAB familial isolated dilated cardiomyopathy · dilated cardiomyopathy type 1II
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