Phenotypes for disease #00817 (MDDGB6 (dystrophy, muscular, dystroglycanopathy (congenital with mental retardation), type B6), OMIM:608840)

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AscendingPhenotype ID     

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0000079477 6m-generalized hypotonia, facial weakness, severe motor delay; 14m-independent ambulation started, but lost at 24m; 11y-low weight and height, weakness and generalized muscular wasting, absence of osteotendinous reflexes, and scoliosis on X-ray chest evaluation - - Familial, autosomal recessive 00y06m >11y 00y06m Generalized hypotonia - Miguel Angel Alcántara-Ortigoza 00101230
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