Desmoid Disease, Hereditary (DESMD)

Alias:
Fif
Familial Infiltrative Fibromatosis
Hereditary Desmoid Disease
Desmd
Fibromatosis, Familial Infiltrative
Fibromatosis, Aggressive
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Desmoid Disease, Hereditary, also known as fif, is related to desmoid tumor and familial adenomatous polyposis 1. An important gene associated with Desmoid Disease, Hereditary is APC (APC Regulator Of WNT Signaling Pathway), and among its related pathways/superpathways are Presenilin action in Notch and Wnt signaling and Deactivation of the beta-catenin transactivating complex. The drugs Sorafenib and Doxorubicin have been mentioned in the context of this disorder. Affiliated tissues include breast and colon, and related phenotypes are desmoid tumors and colorectal polyposis
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
--
11
102
11

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Tutorials
Back to top