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Results 1 - 3 of 3 for Familial hemophagocytic lymphohistiocytosis 3
  1. UNC13D gene 
    ... the most common molecular defect in patients with familial hemophagocytic lymphohistiocytosis type 3. Haematologica. 2008 Jul;93(7):1086-90. doi: ...
    https://medlineplus.gov/genetics/gene/unc13d - Genetics
  2. XIAP gene 
    ... unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease. Blood. ...
    https://medlineplus.gov/genetics/gene/xiap - Genetics
  3. RAB27A gene 
    ... system cells also leads to a condition called hemophagocytic lymphohistiocytosis (HLH) in people with Griscelli syndrome type 2. ...
    https://medlineplus.gov/genetics/gene/rab27a - Genetics