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PedAM

Pediatric Disease Annotations & Medicines




Disease iga glomerulonephritis
Phenotype C0154254|polyclonal hypergammaglobulinemia
Sentences 1
PubMedID- 20335784 A 35-year-old japanese man developed systemic lymphadenopathy during the course of immunosuppressive therapy for iga nephropathy associated with cutaneous nodules, polyclonal hypergammaglobulinemia, and persistent increased serum c-reactive protein of unknown cause.

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