FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term primary ovarian insufficiency 6 ID (Ontology) DOID:0080863 (Human Disease)
Definition A primary ovarian insufficiency that has_material_basis_in heterozygous or homozygous mutation in the FIGLA gene on chromosome 2p13.
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 primary ovarian insufficiency 6       1
 for disease ribbon | primary ovarian insufficiency 6       1
 model of | primary ovarian insufficiency 6       1
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autosomal genetic disease
 |__autosomal dominant disease_____
ovarian disease                    |
 |__primary ovarian insufficiency__|
                                   primary ovarian insufficiency 6  1 rec.
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Is a autosomal dominant disease
primary ovarian insufficiency
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MIM:612310