FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term muscular dystrophy-dystroglycanopathy type B ID (Ontology) DOID:0112375 (Human Disease)
Definition A muscular dystrophy-dystroglycanopathy characterized by early onset of muscle weakness, intellectual disability in most cases, and variable presence of mild brain anomalies.
Also Known As "MDDGB"
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DO.org
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Spanning Tree (Parents/Children)
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  congenital muscular dystrophy
   |__muscular dystrophy-dystroglycanopathy
       |__muscular dystrophy-dystroglycanopathy type B  12 rec.
           |__muscular dystrophy-dystroglycanopathy type B1 3 rec.
           |__muscular dystrophy-dystroglycanopathy type B2 2 rec.
           |__muscular dystrophy-dystroglycanopathy type B3 1 rec.
           |__muscular dystrophy-dystroglycanopathy type B4
           |__muscular dystrophy-dystroglycanopathy type B5 1 rec.
           |__muscular dystrophy-dystroglycanopathy type B6 3 rec.
           |__muscular dystrophy-dystroglycanopathy type B14 1 rec.
           |__muscular dystrophy-dystroglycanopathy type B15 1 rec.
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Is a muscular dystrophy-dystroglycanopathy
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Synonyms
  • "MDDGB" EXACT OMO:0003012
Secondary IDs
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MIM:PS613155