Phenotype #0000025736

Individual ID 00029771
Associated disease POF-8
Phenotype details see paper; ...; primary ovarian insufficiency with complete lack of any pubertal development and streak gonads
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Polona Le Quesne Stabej