CRYAB-related myofibrillar myopathy-cataract-cardiomyopathy spectrum disorder
MONDO:1060212A syndromic disease caused by a variation in the CRYAB gene, and characterized by a spectrum of phenotypes including cardiomyopathy, cataract, and/or myopathy.
Also known as: CRYAB-related myofibrillar myopathy-cataract-cardiomyopathy spectrum disorder, alpha-B crystallinopathy
0 clinical trials for this condition and its sub-types, 0 tagged with CRYAB-related myofibrillar myopathy-cataract-cardiomyopathy spectrum disorder itself.
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Browse by category →Sub-types of CRYAB-related myofibrillar myopathy-cataract-cardiomyopathy spectrum disorder
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Cataract 16 multiple types 0 trials
2 sub-types
- Early-onset lamellar cataract 0 trials
- Early-onset posterior polar cataract 0 trials
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Dilated cardiomyopathy 1II 0 trials
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Myofibrillar myopathy 2 0 trials
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