Diseases evaluated by ALDA Associated gene(s)
LGMD2A/LGMDR1 or LGMD1I/LGMDD4 CAPN3
LGMD2B/LGMDR2 DYSF
LGMD2C/LGMDR5 SGCG
LGMD2D/LGMDR3 SGCA
LGMD2E/LGMDR4 SGCB
LGMD2F/LGMDR6 SGCD
LGMD2G/LGMDR7 TCAP
LGMD2H/LGMDR8 TRIM32
LGMD2I/LGMDR9 FKRP
LGMD2J/LGMDR10 TTN
LGMD2K/LGMDR11 POMT1
LGMD2L/LGMDR12 ANO5
LGMD2M/LGMDR13 FKTN
LGMD2N/LGMDR14 POMT2
LGMD2O/LGMDR15 POMGnT1
LGMD2P/LGMDR16 DAG1
LGMD2Q/LGMDR17 PLEC1
LGMD2U/LGMDR20 ISPD
LGMD1A/Myofibrillar myopathy MYOT
LGMD1B/AD EDMD LMNA
LGMD1C/Rippling muscle disease CAV3
LGMD1D/LGMDD1 DNAJB6
LGMD1E/Myofibrillar myopathy DES
LGMD1F/LGMDD2 TNPO3
LGMD1G/LGMDD3 HNRPDL
LGMD1H unknown
GNE Myopathy GNE
Becker MD DMD
DMD Manifesting Carrier DMD
FSHD D4Z4 microsatellite repeat, SMCHD1
EDMD (X-linked) EMD, FHL1
Pompe/GAA GAA
Collagen VI myopathy/LGMDR22/LGMDD5 COL6A1, A2, or A3

For additional information about the muscular dystrophies evaluated by ALDA, go to the Washington University muscular dystrophy page.