Genopathy
Gene-Disorder Association · Article
Gene
MYD88
MYD88 Innate Immune Signal Transduction Adaptor
Disorder
Waldenstram Macroglobulinemia
First reported 2013
Supporting publications 2
Key publication · disorder MYD88 L265P in Waldenström macroglobulinemia, immunoglobulin M monoclonal gammopathy, and other B-cell lymphoproliferative disorders using conventional and quantitative allele-specific polymerase chain reaction.Blood · 2013
Manually curated
Association Review

In brief

The association between MYD88 (MYD88 Innate Immune Signal Transduction Adaptor) and Waldenstram Macroglobulinemia is a manually-curated gene–disease association, drawing on a single expert-curated source, which records causative variation.

Sources 1
Clinical variants 0
Symptoms 45
Compounds 0
Trials 0
Publications 2
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
03
MYD88

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

Request access
04
Waldenstram Macroglobulinemia

The disorder

6 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

Request access
05
Literature

Reading

2 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

Request access
06
Provenance

References & sources

5 references

Every source and publication cited across this dossier, as one numbered reference list.

Request access