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Results 1 - 5 of 5 for Familial hemophagocytic lymphohistiocytosis 3
  1. Familial hemophagocytic lymphohistiocytosis 
    ... the most common molecular defect in patients with familial hemophagocytic lymphohistiocytosis type 3. Haematologica. 2008 Jul;93(7):1086-90. doi: 10.3324/haematol.12622. Epub 2008 May 19. Citation on PubMed ... of familial haemophagocytic lymphohistiocytosis type 3. J Med Genet. 2011 ...
    https://medlineplus.gov/...milial-hemophagocytic-lymphohistiocytosis - Genetics
  2. 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
  3. 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
  4. X-linked lymphoproliferative disease 
    ... unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease. Blood. ...
    https://medlineplus.gov/.../x-linked-lymphoproliferative-disease - Genetics
  5. 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