PRDM9

PR/SET domain 9
OMIM: 609760, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
No list PRDM9 in Primary ovarian insufficiency

Level 3: Gonadal and sex development disorders
Level 2: Endocrine disorders
Version 1.67

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
Phenotypes
  • Premature ovarian insufficiency