FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term 46 XX gonadal dysgenesis ID (Ontology) DOID:14450 (Human Disease)
Definition A gonadal dysgenesis that is characterized by the lack of functional ovaries to induce puberty in an otherwise 46,XX female.
Also Known As "ovarian dysgenesis"
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DO.org
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       2
Human Disease Models (FBhh)  DOID       1
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 Alleles Genes Human Disease Models
 46 XX gonadal dysgenesis       2      2      1
 model of | 46 XX gonadal dysgenesis       2       --       --
Spanning Tree (Parents/Children)
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  disorder of sexual development
   |__gonadal dysgenesis
       |__46 XX gonadal dysgenesis  18 rec.
           |__ovarian dysgenesis 1 1 rec.
           |__ovarian dysgenesis 2
           |__ovarian dysgenesis 3
           |__ovarian dysgenesis 4 7 rec.
           |__ovarian dysgenesis 5
           |__ovarian dysgenesis 6 3 rec.
           |__ovarian dysgenesis 7 2 rec.
           |__ovarian dysgenesis 8 1 rec.
           |__ovarian dysgenesis 9
           |__ovarian dysgenesis 10
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Is a gonadal dysgenesis
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Synonyms
  • "ovarian dysgenesis" EXACT
Secondary IDs
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MESH:D023961
MIM:PS233300
NCI:C120197
ORDO:243
UMLS_CUI:C0949595