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Autosomal dominant centronuclear myopathy

AD centronuclear myopathyAD CNM
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Type of Disease: Genetic, autosomal dominant Pediatric onset

Trusted Medical Sites

Genetic & Rare Diseases Information Center (GARD) GARD provides the public with access to current, reliable, and easy-to-understand information about rare or genetic diseases in English or Spanish.

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Disease Resources

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Displaying 1-2 of 2 results.
Welcome letter
Added By: Team Titin
Publish Date: Jun 1, 2016
Category: General
Language(s): English
This is a welcome letter for families newly diagnosed with titin related muscle disorders.
Patient Registry
Added By: Team Titin
Added On: Oct 5, 2012
Category: General
Language(s): English, Spanish and more via google translate
A patient registry for people with muscle disorders. The Congenital Muscle Disease International Registry (CMDIR) was created in 2009 to identify the global congenital muscle disease population for the purpose of raising awareness, standards of care,