Gene-Disorder Association · Article
First reported
1990
Supporting publications
76
Manually curatedApproved treatment annotated
Association Review
In brief
The association between CCND1 (Cyclin D1) and Lymphoma is reported, with clinical genetic testing available.
Sources
1
Clinical variants
0
Symptoms
0
Compounds
3
Trials
443of 3,887 via CCND1 compounds
Publications
76
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.
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02
Provenance
Evidence and sources
1 source
Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.
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2 source summaries
A gene summary alongside the source descriptions it was distilled from.
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12 database identifiers
The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).
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05
Population genetics
GWAS signals
1 GWAS phenotype
Gene-associated GWAS phenotypes matching the disorder, with best SNP, score, risk-allele frequency and effect size.
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06
Interventions
Therapeutics
3 compounds & drugs
Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.
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07
Human studies
Clinical trials
3,887 clinical trials
Clinical trials reached through the pair’s compounds, keeping disorder-targeting trials separate from other indications.
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76 publications
Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.
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09
Provenance
References & sources
14 references
Every source and publication cited across this dossier, as one numbered reference list.
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