antiphospholipid syndrome; Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A hypersensitivity reaction type II disease that is characterized by recurrent venous or arterial thrombosis and/or fetal losses associated with characteristic elevated levels of antibodies directed against membrane anionic phospholipids (anticardiolipin). (Human Disease Ontology, DOID_2988)
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Genes

4 genes associated with the disease antiphospholipid syndrome; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
BANK1 B-cell scaffold protein with ankyrin repeats 1
BLK BLK proto-oncogene, Src family tyrosine kinase
IRF5 interferon regulatory factor 5
STAT4 signal transducer and activator of transcription 4