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- B82ba3f68a327dc4a422d827fdfc0cd1e hasDbXref "Orphanet:57782" @default.
- B82ba3f68a327dc4a422d827fdfc0cd1e type Axiom @default.
- B82ba3f68a327dc4a422d827fdfc0cd1e annotatedProperty IAO_0000115 @default.
- B82ba3f68a327dc4a422d827fdfc0cd1e annotatedSource MONDO_0018933 @default.
- B82ba3f68a327dc4a422d827fdfc0cd1e annotatedTarget "Mazabraud syndrome is a rare primary bone dysplasia characterized by the association of fibrous dysplasia with intramuscular myxomas. Fibrous dysplasia (usually polyostotic, sometimes monostotic) occurs during the growth period and can be asymptomatic or can present with pain, skeletal deformities or fractures while intramuscular myxoma, associated with polyostotic fibrous dysplasia is usually multifocal, typically occuring in the vicinity of skeletal lesions, and presents in adulthood as a painless soft-tissue mass (most commonly in the thigh). Although it is a benign condition, local recurrences of myxomas after incomplete excision and malignant transformation of a fibrous dysplastic lesion into osteogenic sarcoma have been reported." @default.