FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
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Term ovarian dysgenesis 1 ID (Ontology) DOID:0080493 (Human Disease)
Definition A 46 XX gonadal dysgenesis that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding follicle-stimulating hormone receptor on chromosome 2p16.
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 Genes
 ovarian dysgenesis 1       1
 for disease ribbon | ovarian dysgenesis 1       1
 model of | ovarian dysgenesis 1       1
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autosomal genetic disease
 |__autosomal recessive disease__
gonadal dysgenesis               |
 |__46 XX gonadal dysgenesis_____|
                                 ovarian dysgenesis 1  1 rec.
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Is a autosomal recessive disease
46 XX gonadal dysgenesis
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MIM:233300