Previous symbols: AS.
Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.
| Disorder | Relationship | Where the gene appears |
|---|---|---|
| Adult-Onset Myasthenia Gravis | susceptibility |
scoped to subtype: EOMG
|
| Allopurinol-Induced Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis | risk factor germline |
mechanism: Oxypurinol-HLA class I interaction with HLA-B*58:01 susceptibility
|
| Autoimmune Hepatitis | risk factor germline |
mechanism: Polygenic HLA-linked susceptibility
|
| Endomyocardial Fibrosis | susceptibility germline | |
| Isoniazid Toxicity | susceptibility | |
| Primary Sclerosing Cholangitis | susceptibility | |
| Uveitis | risk factor |
subtype: HLA-B27-Associated Anterior Uveitis
|
| Giant Cell Arteritis |
untyped
Risk Factor
|
|
| Kawasaki Disease |
untyped
HLA associations support antigen-driven or superantigen-like T-cell responses
|
|
| Takayasu Arteritis |
untyped
Major susceptibility factor
|
|
| Ankylosing Spondylitis | no genetic record |
mechanism: HLA-B27 Misfolding and ER Stress
|
| Stevens-Johnson Syndrome | no genetic record |
mechanism: HLA-Mediated Genetic Susceptibility
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.