Gene-Disorder Association · Article
Gene
HLA-DRB1 Major Histocompatibility Complex, Class II, DR Beta 1
×
First reported
1994
Supporting publications
2
Manually curated Approved treatment annotated
Association Review
In brief The association between HLA-DRB1 (Major Histocompatibility Complex, Class II, DR Beta 1) and Temporal Arteritis is a manually-curated gene–disease association, drawing on a single expert-curated source, which records a susceptibility locus.
Sources
1
Clinical variants
0
Symptoms
89
Compounds
1
Trials
18 of 480 via HLA-DRB1 compounds
Publications
2
Contents
01
At a glance
Association overview A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.
Request access
02
Provenance
Evidence and sources 1 source
Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.
Request access
1 source summary
A gene summary alongside the source descriptions it was distilled from.
Request access
04
Temporal Arteritis
The disorder 21 database identifiers
The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).
Request access
05
Phenotype
Clinical features 71 clinical features
The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.
Request access
06
Population genetics
GWAS signals 1 GWAS phenotype
Gene-associated GWAS phenotypes matching the disorder, with best SNP, score, risk-allele frequency and effect size.
Request access
07
Mechanism overlap
Shared mechanisms Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.
Request access
08
Interventions
Therapeutics 1 compound or drug
Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.
Request access
09
Human studies
Clinical trials 480 clinical trials
Clinical trials reached through the pair’s compounds, keeping disorder-targeting trials separate from other indications.
Request access
2 publications
Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.
Request access
11
Provenance
References & sources 10 references
Every source and publication cited across this dossier, as one numbered reference list.
Request access