MeSH 搜索器

Monoclonal Gammopathy of Undetermined Significance

Conditions characterized by the presence of M protein (Monoclonal protein) in serum or urine without clinical manifestations of plasma cell dyscrasia.
推出的年份: 1991(1986)
副标题
树号: C15.378.147.542.640, C15.378.147.780.570, C20.683.460.640, C20.683.780.640
MeSH 单一 ID: D008998
进入的组:
  • Monoclonal Gammopathies, Benign
  • Monoclonal Gammapathy of Undetermined Significance
  • Benign Monoclonal Gammopathies
  • Benign Monoclonal Gammopathy
  • Monoclonal Gammopathy, Benign
  • Monoclonal Gammapathies, Benign
  • Benign Monoclonal Gammapathies
  • Benign Monoclonal Gammapathy
  • Monoclonal Gammapathy, Benign
早前的内容:
  • Blood Protein Disorders (1966-1968)
  • Hypergammaglobulinemia (1969-1985)

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