All diseases

OMIM ID
174810
OMIM term:
FAMILIAL EXPANSILE OSTEOLYSIS; FEO
Alternative terms:
POLYOSTOTIC OSTEOLYTIC DYSPLASIA, HEREDITARY EXPANSILE; HEPOD
MCCABE DISEASE
EXPANSILE OSTEOLYSIS, FAMILIAL; EOF
(∗) Location:
18q21.33  
(†) Associated OMIM genes:
TNFRSF11A  
(‡) Associated MGI genes:

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