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Up to: Hereditary neurological disease · Congenital nervous system disorder · Disorder of protein O-glycosylation · Neuromuscular disease caused by qualitative or quantitative defects of alpha-dystroglycan
Qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan
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Qualitative or quantitative defects of FKRP 0 trials · 8 incl. sub-types Sub-types →
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Myopathy caused by variation in FKTN 1 trial · 2 incl. sub-types Sub-types →
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Myopathy caused by variation in CRPPA 0 trials · 1 incl. sub-types Sub-types →
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Myopathy caused by variation in GMPPB 0 trials · 1 incl. sub-types Sub-types →
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Myopathy caused by variation in POMT1 0 trials · 1 incl. sub-types Sub-types →
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Myopathy caused by variation in POMT2 0 trials · 1 incl. sub-types Sub-types →
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Qualitative or quantitative defects of protein O-mannosyltransferase 1 0 trials · 1 incl. sub-types Sub-types →
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Qualitative or quantitative defects of protein O-mannosyltransferase 2 0 trials · 1 incl. sub-types Sub-types →