Congenital Disorder of Glycosylation, Type Icc (CDG1CC)

Alias:

Cdg1cc

Glycosylation, Congenital Disorder of, Type Icc

Congenital Disorder of Glycosylation Type Icc

Congenital Disorder of Glycosylation Icc

Congenital Disorder of Glycosylation 1cc

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Congenital Disorder of Glycosylation, Type Icc, is also known as cdg1cc. An important gene associated with Congenital Disorder of Glycosylation, Type Icc is MAGT1 (Magnesium Transporter 1). Related phenotypes are intellectual disability and global developmental delay

Related ID：

MALACARDS：CNG607

OMIM：301031

MESH：D018981