NOBOX

NOBOX oogenesis homeobox
OMIM: 610934, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green NOBOX in Primary ovarian insufficiency

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

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Other
  • Illumina TruGenome Clinical Sequencing Services
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Premature ovarian failure 5,611548
  • Premature Ovarian Failure