FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Denys-Drash syndrome ID (Ontology) DOID:3764 (Human Disease)
Definition A syndrome that is characterized by the association of diffuse mesangial sclerosis (DMS), male pseudohermaphroditism with a 46,XY karyotype, and nephroblastoma that derives_from an abnormality in the WT1 gene (Wilms' tumor suppressor gene).
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 Genes
 Denys-Drash syndrome       1
 for disease ribbon | Denys-Drash syndrome       1
 model of | Denys-Drash syndrome       1
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autosomal genetic disease
 |__autosomal dominant disease__
disease                         |
 |__syndrome____________________|
                                Denys-Drash syndrome  1 rec.
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Is a autosomal dominant disease
syndrome
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Synonyms
Secondary IDs
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GARD:5576
MESH:D030321
MIM:194080
NCI:C84668
SNOMEDCT_US_2023_03_01:236385009
UMLS_CUI:C0950121