FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term nephrotic syndrome type 20 ID (Ontology) DOID:0070357 (Human Disease)
Definition A familial nephrotic syndrome that has_material_basis_in X-linked renal disorder characterized by onset of steroid-resistant nephrotic syndrome and proteinuria in the first years of life in affected males.
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS      10
Human Disease Models (FBhh)  DOID       1
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Relevant FlyBase reports
 Alleles Genes Human Disease Models
 nephrotic syndrome type 20      11      2      1
 ameliorates | nephrotic syndrome type 20       1       --       --
 for disease ribbon | nephrotic syndrome type 20       --       1       --
 model of | nephrotic syndrome type 20      10      1       --
 DOES NOT model | nephrotic syndrome type 20       1       --       --
Spanning Tree (Parents/Children)
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monogenic disease___
nephrotic syndrome__|
                    familial nephrotic syndrome
                     |__nephrotic syndrome type 20  14 rec.
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MIM:301028