FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hereditary desmoid disease ID (Ontology) DOID:0111349 (Human Disease)
Definition A syndrome characterized by extraintestinal manifestation of familial adenomatous polyposis that has_material_basis_in in some cases by extreme 3' mutation in APC on 5q22.2.
Also Known As "familial infiltrative fibromatosis" ; "FIF"
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 Genes
 hereditary desmoid disease       1
 for disease ribbon | hereditary desmoid disease       1
 model of | hereditary desmoid disease       1
Spanning Tree (Parents/Children)
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monogenic disease
 |__autosomal genetic disease__
disease                        |
 |__syndrome___________________|
                               hereditary desmoid disease  1 rec.
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Is a autosomal genetic disease
syndrome
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Synonyms
  • "familial infiltrative fibromatosis" EXACT
    "FIF" EXACT OMO:0003012
Secondary IDs
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MESH:C535944
MIM:135290
UMLS_CUI:C1851124