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Up to: Syndromic disease · Cardiogenetic disease · Developmental anomaly of metabolic origin · Congenital disorder of glycosylation type II · Defect in conserved oligomeric Golgi complex
COG1-congenital disorder of glycosylation
COG1-CDG is an extremely rare form of CDG syndrome characterized clinically in the few cases reported to date by variable signs including microcephaly, growth retardation, psychomotor retardation and facial dysmorphism.
This condition has no sub-types.