COG2

component of oligomeric golgi complex 2
OMIM: 606974, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red COG2 in Congenital Disorders of Glycosylation


Level 2: Metabolic disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Congenital disorder of glycosylation, type IIq (MIM# 617395)

Red COG2 in Mendeliome


Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Congenital disorder of glycosylation, type IIq (MIM# 617395)