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ENMuscular Dystrophy-Dystroglycanopathy , Type a, 10 (MDDGA10)
Alias:
Mddga10
Muscular Dystrophy-Dystroglycanopathy Congenital with Brain and Eye Anomalies A10
Walker-Warburg Syndrome or Muscle-Eye-Brain Disease, Tmem5-Related
Dystrophy, Muscular, Dystroglycanopathy , Type A10
Muscle-Eye-Brain Disease Tmem5-Related
Walker-Warburg Syndrome Tmem5-Related
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Muscular Dystrophy-Dystroglycanopathy , Type a, 10, also known as mddga10, is related to congenital muscular dystrophy-dystroglycanopathy type a10. An important gene associated with Muscular Dystrophy-Dystroglycanopathy , Type a, 10 is RXYLT1 (Ribitol Xylosyltransferase 1). Affiliated tissues include eye and brain, and related phenotypes are retinal dysplasia and type ii lissencephaly
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