FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Frasier syndrome ID (Ontology) DOID:0050438 (Human Disease)
Definition A syndrome that is characterized by gonadal dysgenesis, streak gonads, progressive focal segmental glomerulonephropathy and the development of urogenital cancers that is the result of mutation in the WT1 gene.
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 Genes
 Frasier syndrome       1
 for disease ribbon | Frasier syndrome       1
 model of | Frasier syndrome       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
disease                         |
 |__syndrome____________________|
                                Frasier 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:2375
MESH:D052159
MIM:136680
NCI:C122805
SNOMEDCT_US_2023_03_01:445431000
UMLS_CUI:C0950122