Muscular dystrophy-dystroglycanopathy, type A
MONDO:0000171Also known as: WWS, Walker-Warburg muscular dystrophy, Walker-Warburg syndrome, hard syndrome, hydrocephalus-agyria-retinal dysplasia syndrome, Chemke syndrome, Pagon syndrome, Warburg syndrome
40 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
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Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10
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Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
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Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12
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Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13
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Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14
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Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2
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Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3
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Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4
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Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5
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Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6
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Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7
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Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8
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Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9
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