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ENCongenital Muscular Dystrophy-Dystroglycanopathy A7
Alias:
Congenital Muscular Dystrophy-Dystroglycanopathy with Brain and Eye Anomalies, Type A7
Congenital Muscular Dystrophy-Dystroglycanopathy with Brain and Eye Anomalies Type A7
Walker-Warburg Syndrome or Muscle-Eye-Brain Disease Ispd-Related
Mddga7
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Congenital Muscular Dystrophy-Dystroglycanopathy A7, also known as congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type a7, is related to muscular dystrophy-dystroglycanopathy , type a, 7 and muscular dystrophy-dystroglycanopathy , type a, 8. An important gene associated with Congenital Muscular Dystrophy-Dystroglycanopathy A7 is CRPPA (CDP-L-Ribitol Pyrophosphorylase A). Affiliated tissues include eye and brain.
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