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 3 ID (Ontology) DOID:0080382 (Human Disease)
Definition A familial nephrotic syndrome characterized by early childhood onset, steroid restance and diffuse mesangial sclerosis in most patients that has_material_basis_in homozygous or compound heterozygous mutation in the PLCE1 gene on chromosome 10q23.
Also Known As "early onset nephrotic syndrome type 3"
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 Genes
 nephrotic syndrome type 3       1
 for disease ribbon | nephrotic syndrome type 3       1
 model of | nephrotic syndrome type 3       1
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monogenic disease
 |__familial nephrotic syndrome__
autosomal genetic disease        |
 |__autosomal recessive disease__|
nephrotic syndrome               |
 |__familial nephrotic syndrome__|
                                 nephrotic syndrome type 3  1 rec.
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Is a autosomal recessive disease
familial nephrotic syndrome
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Synonyms
  • "early onset nephrotic syndrome type 3" EXACT
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MIM:610725