MeSH Browser

MeSH Supplementary: Desmoid disease, hereditary
Unique ID: C535944
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535944
Entry Term(s): Desmoid Tumor Caused By Somatic Mutation; Familial infiltrative fibromatosis; Fibromatosis, familial infiltrative
Registry Number: 0
Heading Mapped to: *Abdominal Neoplasms; *Adenomatous Polyposis Coli; *Fibromatosis, Aggressive
Frequency: 30
Note: Benign extraintestinal desmoid tumors (FIBROMATOSIS, ABDOMINAL) that are often associated with familial adenomatous polyposis. They may be caused by hereditary mutations in the APC gene or spontaneuos mutations in the BETA-CATENIN (CTNNB1) gene. OMIM: 135290
Date of Entry: 2010/08/25
Revision Date: 2016/09/29

Desmoid disease, hereditary MeSH Supplementary Concept Data 2024