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Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II [Supplementary Concept]

mutation in NCF2

Date introduced: November 5, 2012

MeSH Unique ID: C565531

Heading Mapped to:

Entry Terms:

  • P67-Phox, Deficiency of
  • Neutrophil Cytosol Factor 2, Deficiency of
  • CGD, Autosomal Recessive Cytochrome B-Positive, Type II
  • Granulomatous Disease, Chronic, due to NCF2 Deficiency

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