Congenital Disorder of Glycosylation, Type Iw, Autosomal Dominant (CDG1WAD)

Congenital Disorder of Glycosylation, Type Iw, Autosomal Dominant(来自ICD-11)

别称:

Cdg1wad

Congenital Disorder of Glycosylation 1w, Autosomal Dominant

加入收藏

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Congenital Disorder of Glycosylation, Type Iw, Autosomal Dominant, is also known as cdg1wad. An important gene associated with Congenital Disorder of Glycosylation, Type Iw, Autosomal Dominant is STT3A (STT3 Oligosaccharyltransferase Complex Catalytic Subunit A). Affiliated tissues include skeletal muscle, and related phenotypes are motor delay and intellectual disability

查看原文参与反馈