Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Browse

Explore conditions, clinical trials, and the organisations running them.

← All categories

Up to: Hereditary disease · Syndromic disease

CRYAB-related myofibrillar myopathy-cataract-cardiomyopathy spectrum disorder

A syndromic disease caused by a variation in the CRYAB gene, and characterized by a spectrum of phenotypes including cardiomyopathy, cataract, and/or myopathy.

0 trials tagged with this condition →