Additional Disease Briefs
autosomal recessive limb-girdle muscular dystrophy type 2A
Also known as: CAPN3 autosomal recessive limb-girdle muscular dystrophy, LGMD2, LGMD2A, Leyden-Moebius muscular dystrophy, autosomal recessive limb-girdle muscular dystrophy caused by mutation in CAPN3, autosomal recessive limb-girdle muscular dystrophy type 2A, calpainopathy, limb-girdle muscular dystrophy due to calpain deficiency, limb-girdle muscular dystrophy type 2, limb-girdle muscular dystrophy type 2A, muscular dystrophy limb girdle type 2A, erb type, muscular dystrophy, Pelvofemoral, muscular dystrophy, limb-girdle, autosomal recessive 1, muscular dystrophy, limb-girdle, type 2, muscular dystrophy, limb-girdle, type 2A, myositis, eosinophilic, pelvofemoral muscular dystrophy, primary calpainopathy
autosomal recessive limb-girdle muscular dystrophy type 2B
Also known as: DYSF autosomal recessive limb-girdle muscular dystrophy, LGMD2B, LGMD3, autosomal recessive limb-girdle muscular dystrophy caused by mutation in DYSF, limb-girdle muscular dystrophy due to dysferlin deficiency, limb-girdle muscular dystrophy type 2B, limb-girdle muscular dystrophy type 3, limb-girdle muscular dystrophy, type 2B, muscular dystrophy, limb-girdle, autosomal recessive 2, muscular dystrophy, limb-girdle, type 2B, muscular dystrophy, limb-girdle, type 3
autosomal recessive limb-girdle muscular dystrophy type 2C
Also known as: Adhalin deficiency, secondary, DMDA1, Dmda, Duchenne-like muscular dystrophy, autosomal recessive, type 1, LGMD2C, Maghrebian myopathy, SCARMD, SGCG autosomal recessive limb-girdle muscular dystrophy, autosomal recessive Duchenne-like muscular dystrophy type 1, autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCG, autosomal recessive limb-girdle muscular dystrophy type 2C, deficiency of sarcoglycan gamma, gamma-sarcoglycanopathy, limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency, limb-girdle muscular dystrophy with gamma-sarcoglycan deficiency, limb-girdle muscular dystrophy, type 2C, muscular dystrophy, Duchenne-like, muscular dystrophy, limb-girdle, autosomal recessive 5, muscular dystrophy, limb-girdle, type 2C, sarcoglycan, gamma, deficiency of, severe childhood autosomal recessive muscular dystrophy North African type, severe childhood autosomal recessive muscular dystrophy, North African type
autosomal recessive limb-girdle muscular dystrophy type 2D
Also known as: Adhalinopathy, primary, Alpha-sarcoglycanopathy, DMDA2, Duchenne-like autosomal recessive muscular dystrophy type 2, Duchenne-like autosomal recessive muscular dystrophy, type 2, LGMD2D, SGCA autosomal recessive limb-girdle muscular dystrophy, autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCA, limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency, limb-girdle muscular dystrophy type 2D, limb-girdle muscular dystrophy, type 2D, muscular dystrophy limb-girdle with alpha-sarcoglycan, muscular dystrophy, limb-girdle, autosomal recessive 3, muscular dystrophy, limb-girdle, type 2D, primary adhalinopathy
autosomal recessive limb-girdle muscular dystrophy type 2E
Also known as: LGMD due to beta-sarcoglycan deficiency, LGMD type 2E, LGMD2E, LGMDR4, SGCB autosomal recessive limb-girdle muscular dystrophy, autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCB, autosomal recessive limb-girdle muscular dystrophy type 2E, beta-sarcoglycan limb-girdle muscular dystrophy, beta-sarcoglycan-related LGMD R4, beta-sarcoglycan-related limb-girdle muscular dystrophy R4, beta-sarcoglycanopathy, limb-girdle muscular dystrophy due to beta-sarcoglycan deficiency, limb-girdle muscular dystrophy type 2E, muscular dystrophy limb-girdle with beta-sarcoglycan deficiency, muscular dystrophy, limb-girdle, autosomal recessive 4, muscular dystrophy, limb-girdle, type 2E
autosomal recessive limb-girdle muscular dystrophy type 2F
Also known as: LGMD2F, SGCD autosomal recessive limb-girdle muscular dystrophy, autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCD, delta-sarcoglycanopathy, limb-girdle muscular dystrophy due to delta-sarcoglycan deficiency, limb-girdle muscular dystrophy type 2F, muscular dystrophy limb-girdle with delta-sarcoglyan deficiency, muscular dystrophy, limb-girdle, autosomal recessive 6, muscular dystrophy, limb-girdle, type 2F
autosomal recessive limb-girdle muscular dystrophy type 2G
Also known as: LGMD2G, TCAP autosomal recessive limb-girdle muscular dystrophy, Tcap autosomal recessive limb-girdle muscular dystrophy, autosomal recessive limb-girdle muscular dystrophy caused by mutation in TCAP, autosomal recessive limb-girdle muscular dystrophy caused by mutation in Tcap, limb-girdle muscular dystrophy due to telethonin deficiency, limb-girdle muscular dystrophy, type 2G, muscular dystrophy, limb-girdle, autosomal recessive 7, muscular dystrophy, limb-girdle, type 2G
autosomal recessive limb-girdle muscular dystrophy type 2H
Also known as: LGMD2H, Sarcotubular myopathy, TRIM32 autosomal recessive limb-girdle muscular dystrophy, autosomal recessive limb-girdle muscular dystrophy caused by mutation in TRIM32, autosomal recessive limb-girdle muscular dystrophy type 2H, limb-girdle muscular dystrophy due to TRIM32 deficiency, limb-girdle muscular dystrophy type 2H, muscular dystrophy Hutterite type, muscular dystrophy limb-girdle type 2H, muscular dystrophy, Hutterite type, muscular dystrophy, limb-girdle, autosomal recessive 8, muscular dystrophy, limb-girdle, type 2H, sarcotubular myopathy
autosomal recessive limb-girdle muscular dystrophy type 2I
Also known as: FKRP autosomal recessive limb-girdle muscular dystrophy, LGMD-FKRP related, LGMD2I, MDDGC5, autosomal recessive limb-girdle muscular dystrophy caused by mutation in FKRP, limb-girdle muscular dystrophy due to FKRP deficiency, limb-girdle muscular dystrophy type 2I, muscular dystrophy limb-girdle type 2I, muscular dystrophy, limb-girdle, type 2I, muscular dystrophy-dystroglycanopathy (Limb-girdle) type C, 5, muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5, muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5, muscular dystrophy-dystroglycanopathy (limb-girdle), type C5, muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related, muscular dystrophy-dystroglycanopathy, limb-girdle, Frkp-related