C14orf39

chromosome 14 open reading frame 39
OMIM: 617307, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green C14orf39 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 Green
  • Literature
Phenotypes
  • ?Premature ovarian failure 18, OMIM:619203