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Ontology Term : Congenital muscular dystrophy UniProtKeyword

description  The congenital muscular dystrophies (CMD) are a heterogeneous group of disorders characterized by hypotonia, muscle weakness, dystrophic changes on skeletal muscle biopsy, and joint contractures that present at birth or during the first 6 months of life. Intellectual disability with or without structural brain changes is an additional feature of several CMD syndromes
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Ontology Term --> Direct children

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