Disease ID | Source | Name | Description |
300510 | OMIM | Ovarian dysgenesis 2 (ODG2) | A disorder characterized by lack of spontaneous pubertal development, primary amenorrhea, uterine hypoplasia, and hypergonadotropic hypogonadism as a result of streak gonads. The disease is caused by variants affecting the gene represented in this entry. |
300510 | OMIM | Ovarian dysgenesis 2 (ODG2) | A disorder characterized by lack of spontaneous pubertal development, primary amenorrhea, uterine hypoplasia, and hypergonadotropic hypogonadism as a result of streak gonads. The disease is caused by variants affecting the gene represented in this entry. |