OBO ID: DOID:0111349
Term Name: hereditary desmoid disease Search Ontology:
Synonyms:
  • familial infiltrative fibromatosis
  • FIF
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. https://www.ncbi.nlm.nih.gov/pubmed/10782927
References:
Ontology: Human Disease   ( DOID:0111349 )
Relationships
is a type of:
OTHER hereditary desmoid disease PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
APC Desmoid disease, hereditary 135290
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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