Familial Expansile Osteolysis (FEO)

Alias:
Mccabe Disease
Hereditary Expansile Polyostotic Osteolytic Dysplasia
Osteolysis, Familial Expansile
Feo
Polyostotic Osteolytic Dysplasia, Hereditary Expansile
Expansile Osteolysis, Familial
Hepod
Eof
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Familial Expansile Osteolysis, also known as mccabe disease, is related to paget's disease of bone 2 and paget disease of bone 2, early-onset. An important gene associated with Familial Expansile Osteolysis is TNFRSF11A (TNF Receptor Superfamily Member 11a), and among its related pathways/superpathways are BAFF in B-Cell Signaling and Apoptosis and survival Anti-apoptotic TNFs/NF-kB/Bcl-2 pathway. Affiliated tissues include bone and cortex, and related phenotypes are conductive hearing impairment and osteolysis
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Child
--
18
167
13

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