Autoimmune Lymphoproliferative Syndrome Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A hypersensitivity reaction type IV disease that is an inherited disorder in which the body cannot properly regulate the number of immune system cells (lymphocytes). It is characterized by the production of an abnormally large number of lymphocytes. Accumulation of excess lymphocytes results in enlargement of the lymph nodes, the liver, and the spleen. (Human Disease Ontology, DOID_6688)
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Genes

4 genes associated with the Autoimmune Lymphoproliferative Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
FAS Fas cell surface death receptor
SH2D1A SH2 domain containing 1A
TNFRSF6B tumor necrosis factor receptor superfamily, member 6b, decoy
UNC13D unc-13 homolog D (C. elegans)