Catalog
Disorders of multiple glycosylation or other pathways
Link to WHO Definition
Disorders of multiple glycosylation or other pathways – http://id.who.int/icd/entity/684473574
Parents
Children
- Conserved oligomeric Golgi complex deficiencies
- V-ATPase deficiencies
- Mannose-P-dolichol utilisation defect 1
- Beta-1,4-galactosyltransferase deficiency
- Hereditary inclusion body myositis
- Leukocyte adhesion deficiency type 2
- Dolichol kinase deficiency
- CMP-sialic acid transporter deficiency
- Dolichol-phosphate-mannose synthase 1 deficiency