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autosomal recessive limb-girdle muscular dystrophy type 2I
MONDO:0011787
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5
MONDO:0013157
limb-girdle muscular dystrophy due to POMK deficiency
MONDO:0014489
qualitative or quantitative defects of protein O-mannosyltransferase 1
MONDO:0016184
qualitative or quantitative defects of protein O-mannosyltransferase 2
MONDO:0016185
myopathy caused by variation in CRPPA
MONDO:0100530