FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term focal segmental glomerulosclerosis 7 ID (Ontology) DOID:0111132 (Human Disease)
Definition A focal segmental glomerulosclerosis that has_material_basis_in an autosomal dominant mutation of the PAX2 gene on chromosome 10q24.31.
Also Known As "FSGS7"
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 Genes
 focal segmental glomerulosclerosis 7       2
 for disease ribbon | focal segmental glomerulosclerosis 7       2
 model of | focal segmental glomerulosclerosis 7       2
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__________
glomerulosclerosis                      |
 |__focal segmental glomerulosclerosis__|
                                        focal segmental glomerulosclerosis 7  2 rec.
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Is a autosomal dominant disease
focal segmental glomerulosclerosis
Part of
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Synonyms
  • "FSGS7" EXACT OMO:0003012
Secondary IDs
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ICD10CM:N04.1
MIM:616002