Congenital Disorder of Glycosylation, Type Iim (CDG2M)

Alias:

Congenital Disorder of Glycosylation Type Iim

Cdg2m

Epileptic Encephalopathy, Early Infantile, 22

Slc35a2-Cdg

Cdg-Iim

Developmental and Epileptic Encephalopathy 22

Congenital Disorder of Glycosylation Type 2m

Slc35a2-Congenital Disorder of Glycosylation

Cdg Syndrome Type Iim

Cdg Iim

Cdgiim

Eiee22

Dee22

Glycosylation, Congenital Disorder of, Type Iim

Congenital Disorder of Glycosylation X-Linked

Congenital Disorder of Glycosylation 2m

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Congenital Disorder of Glycosylation, Type Iim, also known as congenital disorder of glycosylation type iim, is related to congenital disorder of glycosylation, type in and immunodeficiency 47, and has symptoms including seizures An important gene associated with Congenital Disorder of Glycosylation, Type Iim is SLC35A2 (Solute Carrier Family 35 Member A2), and among its related pathways/superpathways are Infectious disease and PAK Pathway. Affiliated tissues include brain and cerebellum, and related phenotypes are intellectual disability and seizure

Related ID：

MALACARDS：CNG389

OMIM：300896

MESH：D013036