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Up to: Congenital disorder of glycosylation · Glycoprotein metabolism disease
Disorder of protein O-glycosylation
A disease that has its basis in the disruption of protein O-linked glycosylation.
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Myopathy caused by variation in FKRP 0 trials · 8 incl. sub-types Sub-types →
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Qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan 0 trials · 8 incl. sub-types Sub-types →
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Disorder of fucoglycosan synthesis 0 trials · 4 incl. sub-types Sub-types →
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Myopathy caused by variation in POMGNT1 0 trials · 1 incl. sub-types Sub-types →