1. Genes and Genomic Entities
  2. SGO2

SGO2

shugoshin 2
OMIM: 612425, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber SGO2 in Primary ovarian insufficiency

Level 3: Gonadal and sex development disorders
Level 2: Endocrine disorders
Version 1.68

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • PERRAULT SYNDROME