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- B2d648d9c921e8e8a2c277651ead871bd hasDbXref "Orphanet:238505" @default.
- B2d648d9c921e8e8a2c277651ead871bd type Axiom @default.
- B2d648d9c921e8e8a2c277651ead871bd annotatedProperty IAO_0000115 @default.
- B2d648d9c921e8e8a2c277651ead871bd annotatedSource MONDO_0016536 @default.
- B2d648d9c921e8e8a2c277651ead871bd annotatedTarget "A rare combined T and B cell immunodeficiency with a predisposition to lymphoproliferative syndrome. It is characterized by persistent symptomatic EBV-viremia and hypogammaglobulinemia variably presenting with fever, lymphadenopathy and systemic inflammatory conditions including hepatitis, pneumonia and sepsis. It may be associated with lymphoma, hemophagocytic lymphohistiocytosis, and aplastic anemia." @default.