|OBO ID: DOID:0111349|
|Term Name:||hereditary desmoid disease||Search Ontology:|
|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|
|Ontology:||Human Disease (DOID:0111349)|
|is a type of:||
OTHER hereditary desmoid disease PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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