STX11base: Familial haemophagocytic lymphohistiocytosis 4

Version 1.0 last updated 16 June, 2011 contains 19 public entries


Curated:	Mauno Vihinen
Maintained by:	Jouni Väliaho
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Short description of the STX11base :

Familial hemophagocytic lymphohistiocytosis is a lethal disorder of immune regulation. It is a disorder of early childhood characterized by excessive, uncontrolled T-lymphocyte and macrophage activation. Infiltration of the liver, spleen, bone marrow, and central nervous system by activated T cells and macrophages results in a multisystem disorder.

Other IBT bioinformatics services:
Immunodeficiency Resource (IDR)
Immunodeficiency Mutation Databases (MUTbase)
IDdiagnostics
Immunome Knowledge Base (IKB) - An integrated service for immunome research
SH2base - Database for pathogenic SH2 domain mutations

IDbases are linked to University of California Santa Cruz (UCSC) genome browser: STX11base