LGMD Subtype (if known)(Required) LGMD 2A / LGMD R1 calpain3-related LGMD 2B / LGMD R2 dysferlin-related LGMD 2C / LGMD R5 y-sarcoglycan-related LGMD 2D / LGMD R3 a-sarcoglycan-related LGMD 2E / LGMD R4 b-sarcoglycan-related LGMD 2F / LGMD R6 d-sarcoglycan-related LGMD 2G / LGMD R7 telethonin-related LGMD 2H / LGMD R8 TRIM32-related LGMD 2I / LGMD R9 FKRP-related LGMD 2J / LGMD R10 titin-related LGMD 2K / LGMD R11 POMT1- related LGMD 2L / LGMD R12 anoctamin5- related LGMD 2M / LGMD R13 Fukutin-related LGMD 2N / LGMD R14 POMT2- related LGMD 2O / LGMD R15 POMGnT1-related LGMD 2P / LGMD R16 a-dystroglycan-related LGMD 2Q / LGMD R17 plectin-related LGMD 2R / / Myofibrillar Myopathy LGMD 2S / LGMD R18 TRAPPC11- related LGMD 2T / LGMD R19 GMPPB-related LGMD 2U / LGMD R20 ISPD-related LGMD 2V / Pompe Disease LGMD 2W / PINCH-2 related myopathy LGMD 2X / BVES-related myopathy LGMD 2Y / TOR1AIP1-related myopathy LGMD 2Z / LGMD R21 POGLUT1-related LGMD R22 Collagen 6-related (Bethlem myopathy recessive) LGMD R23 LAMA2-related LGMD R24 POMNGT2-related LGMD R25 POPDC1-related LGMD R26 POPDC3-related LGMD R27 JAG2-related LGMD R28 HMGCR-related LGMD R29 SNUPN-related LGMD 1A / Myofibrillar Myopathy LGMD 1B / Emery-Dreifuss Muscular Dystrophy (EDMD) LGMD 1C / Rippling Muscle Disease LGMD 1D / LGMD D1 DNAJB6- related LGMD 1E / Myofibrillar Myopathy LGMD 1F / LGMD D2 TNP03- related LGMD 1G / LGMD D3 HNRNPDL-related LGMD 1H / LGMD 1I / LGMD D4 calpain3-related LGMD D5 Collagen 6-related (Bethlem myopathy dominant) Other
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