| umls-concept:C0272199 | skos:definition | NCI: A rare, life-threatening disorder usually appearing during the first few months of life. It is caused by abnormalities in the PRF1, UNC13D, and STX11 genes. It is characterized by histiocytic proliferation and phagocytosis. Patients present with fever, lymphadenopathy, and hepatosplenomegaly.,MSH: Rare form of hemophagocytic lymphohistiocytosis with multiorgan involvement seen in infants and young children | lld:umls |
