FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
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Term primary ovarian insufficiency 15 ID (Ontology) DOID:0080872 (Human Disease)
Definition A primary ovarian insufficiency that is characterized by onset of oligomenorrhea in the third decade of life, with small ovaries, reduced number of follicles, and elevated gonadotropic hormones and that has_material_basis_in homozygous mutation in the FANCM gene on chromosome 14q21.
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 primary ovarian insufficiency 15       1
 for disease ribbon | primary ovarian insufficiency 15       1
 model of | primary ovarian insufficiency 15       1
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autosomal genetic disease
 |__autosomal recessive disease____
ovarian disease                    |
 |__primary ovarian insufficiency__|
                                   primary ovarian insufficiency 15  1 rec.
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Is a autosomal recessive disease
primary ovarian insufficiency
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MIM:618096