Solute carrier family 35 member A2 congenital disorder of glycosylation

Solute carrier family 35 member A2 congenital disorder of glycosylation (disorder)

active

Code	`771516000`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20190131

Synonyms

CDG2M - congenital disorder of glycosylation type 2m
Congenital disorder of glycosylation type 2m
Congenital disorder of glycosylation type IIm
SLC35A2-CDG - solute carrier family 35 member A2 congenital disorder of glycosylation

Parents (6)

277894008Carbohydrate-deficient glycoprotein syndrome type II disorder
1275631007Developmental and epileptic encephalopathy disorder
363070008Developmental hereditary disorder disorder
128190004Inherited metabolic disorder of nervous system disorder
50122000Metabolic encephalopathy disorder
128430005X-linked hereditary disease disorder

Children (0)

None (leaf concept).