1 Child Term
Identifier | Name | Description |
---|---|---|
DOID:0080866 | primary ovarian insufficiency 9 | A primary ovarian insufficiency that has_material_basis_in compound heterozygous mutation in the HFM1 gene on chromosome 1p22. |
1 Parent Term
Identifier | Name | Description |
---|---|---|
DOID:1100 | ovarian disease | A female reproductive system disease that is located_in the ovary. |