Congenital Disorder of Glycosylation, Type Iiaa (CDG2AA)
Alias:
Cdg Iiaa
Cdgiiaa
Cdg2aa
Create a favorites folder
Add To Favorites
Select a favorites
Description
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Disorder of Glycosylation, Type Iiaa, is also known as cdg iiaa. An important gene associated with Congenital Disorder of Glycosylation, Type Iiaa is STX5 (Syntaxin 5). Affiliated tissues include liver and lung.