Familial hemophagocytic lymphohistiocytosis

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Name:
Familial hemophagocytic lymphohistiocytosis
Description:
Familial Hemophagocytic lymphohistiocytosis (FHL) is a rare primary immunodeficiency characterized by a macrophage activation syndrome (see this term) with an onset usually occurring within a few months or less common several years after birth.
ORPHAcode:
540
Synonyms:
Familial HLH
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14