hereditary desmoid disease

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Summary

Literature (0)

DOID:0111349 - hereditary desmoid disease

Disease 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.

Synonyms: familial infiltrative fibromatosis, FIF

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: apc

MIM:

MIM:135290 - DESMOID DISEASE, HEREDITARY; DESMD

MIM:135290 - DESMOID DISEASE, HEREDITARY; DESMD

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal genetic disease (is_a), syndrome (is_a)