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Disease Ontology Browser
familial expansile osteolysis (DOID:0111542)
Alliance: disease page
Synonyms: FEO; hereditary expansile polyostotic osteolytic dysplasia; McCabe disease
Alt IDs: OMIM:174810, MESH:C536335, ORDO:85195, UMLS_CUI:C0432292
Definition: A bone remodeling disease characterized by increased bone remodeling with osteolytic lesions mainly affecting the appendicular skeleton, bone pain, pathological fractures, childhood onset of conductive hearing loss, and premature tooth loss that has_material_basis_in heterozygous mutation in the TNFRSF11A gene on chromosome 18q21.33.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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12/17/2024
MGI 6.24 		The Jackson Laboratory