(Q32147713)

English

congenital generalized lipodystrophy type 4

A congenital generalized lipodystrophy that has material basis in an autosomal recessive mutation of PTRF on chromosome 17q21.2.

  • generalized congenital lipodystrophy with myopathy
  • Brunzell syndrome AGPAT2-related
  • BSCL4
  • GCL4
  • CGL4
  • generalized congenital lipodystrophy type 4
  • Berardinelli-Seip congenital lipodystrophy type 4 with muscular dystrophy
  • Lipodystrophy, Berardinelli-Seip Congenital, Type 4, With Muscular Dystrophy
  • LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4
  • Berardinelli-Seip Congenital Lipodystrophy, Type 4, With Muscular Dystrophy
  • LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4

Statements

0 references
0 references

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit