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- B3a97a19c1f16fe8bf5df2cea26168b62 hasDbXref "Orphanet:1310" @default.
- B3a97a19c1f16fe8bf5df2cea26168b62 type Axiom @default.
- B3a97a19c1f16fe8bf5df2cea26168b62 annotatedProperty IAO_0000115 @default.
- B3a97a19c1f16fe8bf5df2cea26168b62 annotatedSource MONDO_0007244 @default.
- B3a97a19c1f16fe8bf5df2cea26168b62 annotatedTarget "Caffey disease is an osteosclerotic dysplasia characterized by acute inflammation with massive subperiosteal new bone formation usually involving the diaphyses of the long bones, as well as the ribs, mandible, scapulae, and clavicles. The disease is associated with fever, irritability pain and soft tissue swelling, with onset around the age of 2 months and resolving spontaneously by the age of 2 years. However, prenatal disease onset has also been described." @default.