FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term ovarian dysgenesis 6 ID (Ontology) DOID:0080498 (Human Disease)
Definition A 46 XX gonadal dysgenesis that has_material_basis_in homozygous mutation in the NUP107 gene on chromosome 12q15.
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       1
Human Disease Models (FBhh)  DOID       1
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 Alleles Genes Human Disease Models
 ovarian dysgenesis 6       1      1      1
 for disease ribbon | ovarian dysgenesis 6       --       1       --
 model of | ovarian dysgenesis 6       1      1       --
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
gonadal dysgenesis               |
 |__46 XX gonadal dysgenesis_____|
                                 ovarian dysgenesis 6  3 rec.
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Is a autosomal recessive disease
46 XX gonadal dysgenesis
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MIM:618078