Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13
MONDO:0014120Also known as: MDDGA13, Walker-Warburg syndrome or muscle-eye-brain disease, B3Gnt1-related, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13
5 clinical trials for this condition and its sub-types, 0 tagged with Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13 itself.
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Including sub-types (5)
Tagged with Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13 (0)
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