SGO2

shugoshin 2
OMIM: 612425, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red SGO2 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Perrault syndrome

Red SGO2 in Primary Ovarian Insufficiency_Premature Ovarian Failure

Level 3: Gonadal and sex development disorders
Level 2: Endocrine disorders
Version 0.328

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Genetic Health QLD
Phenotypes
  • Perrault syndrome