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autosomal recessive limb-girdle muscular dystrophy type 2K
MONDO:0012248
limb-girdle muscular dystrophy due to POMK deficiency
MONDO:0014489
qualitative or quantitative defects of FKRP
MONDO:0016156
qualitative or quantitative defects of protein O-mannosyltransferase 2
MONDO:0016185
myopathy caused by variation in CRPPA
MONDO:0100530
myopathy caused by variation in FKTN
MONDO:0700067