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familial expansile osteolysis

Disease Summary
Associated Targets (1)
Tbio

1


Explore Associated Targets
Uniprot Description Rare autosomal dominant bone disorder characterized by focal areas of increased bone remodeling. The osteolytic lesions develop usually in the long bones during early adulthood. FEO is often associated with early-onset deafness and loss of dentition.
Mondo Term and Equivalent IDs
MONDO:0008275:  familial expansile osteolysis
DOID:0111542: 
GARD:0009168: 
MESH:C536335: 
Orphanet:85195: 
SCTID:254153009: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)