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ENCongenital Muscular Dystrophy-Dystroglycanopathy Type A10
Alias:
Congenital Muscular Dystrophy-Dystroglycanopathy with Brain and Eye Anomalies Type A10
Walker-Warburg Syndrome or Muscle-Eye-Brain Disease, Tmem5-Related
Mddga10
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Congenital Muscular Dystrophy-Dystroglycanopathy Type A10, also known as congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type a10, is related to muscular dystrophy-dystroglycanopathy , type a, 10 and congenital myopathy 13. An important gene associated with Congenital Muscular Dystrophy-Dystroglycanopathy Type A10 is SELENON (Selenoprotein N). Affiliated tissues include eye and brain.
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