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GTR Home > Conditions/Phenotypes > COG7 congenital disorder of glycosylation


CDG IIe is caused by a mutation that impairs the integrity of the conserved oligomeric Golgi (COG) complex and alters Golgi trafficking, resulting in the disruption of multiple glycosylation pathways. For a general discussion of CDGs, see CDG1A (212065). [from OMIM]

Available tests

35 tests are in the database for this condition.

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Genes See tests for all associated and related genes

  • Also known as: CDG2E, COG7
    Summary: component of oligomeric golgi complex 7

Clinical features


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