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- Bf06652575395b8d5c8d076b72f35ea0e hasDbXref "Orphanet:482" @default.
- Bf06652575395b8d5c8d076b72f35ea0e type Axiom @default.
- Bf06652575395b8d5c8d076b72f35ea0e annotatedProperty IAO_0000115 @default.
- Bf06652575395b8d5c8d076b72f35ea0e annotatedSource MONDO_0018830 @default.
- Bf06652575395b8d5c8d076b72f35ea0e annotatedTarget "Kimura disease is a benign and chronic inflammatory disorder of unknown etiology, occurring mainly in Asian countries (very rarely in Western countries) and predominantly affecting young men, that usually presents with a solitary or multiple non-tender subcutaneous masses in the head and neck region (in particular the preauricular and submandibular area) and/or generalized painless lymphadenopathy, often with salivary gland involvement. Characteristic laboratory findings include blood eosinophilia and markedly elevated serum immunoglobulin E (IgE) levels. It is often associated with autoinflammatory disorders (i.e. ulcerative colitis, bronchial asthma) and a co-existing renal disease." @default.