(Q27677713)

English

autosomal recessive limb-girdle muscular dystrophy type 2T

autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous or compound heterozygous mutation in the GMPPB gene encoding the beta subunit of GDP-mannose pyrophosphorylase on chromosome 3p21

  • LGMD2T
  • MDDGC14
  • muscular dystrophy limb-girdle type 2T
  • muscular dystrophy-dystroglycanopathy (limb-girdle) type C14
  • muscular dystrophy-dystroglycanopathy limb-girdle GMPPB-related
  • Muscular Dystrophy-Dystroglycanopathy, Limb-Girdle, Gmppb-Related
  • Muscular Dystrophy, Limb-Girdle, Type 2T
  • MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14
  • MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14

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