Genopathy
Gene-Disorder Association · Article
Gene
IGHM
Immunoglobulin Heavy Constant Mu
Disorder
Agammaglobulinemia 1, Autosomal Recessive
First reported 2002
Supporting publications 3
Key publication · gene–disorder Clinical and molecular analysis of patients with defects in micro heavy chain gene.The Journal of clinical investigation · 2002
Key publication · disorder Primary 'acquired hypogammaglobulinaemia': a suggested mode of inheritance.Clinical and experimental immunology · 1969
Manually curated
Association Review

In brief

The association between IGHM (Immunoglobulin Heavy Constant Mu) and Agammaglobulinemia 1, Autosomal Recessive is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and likely-pathogenic variants.

Sources 3
Clinical variants 13
Symptoms 27
Compounds 0
Trials 0
Publications 3
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

3 sources

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

Request access
03
IGHM

The gene

1 source summary

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

Request access
04
Agammaglobulinemia 1, Autosomal Recessive

The disorder

7 database identifiers

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

Request access
05
Phenotype

Clinical features

16 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

Request access
06
ClinVar and variant evidence

Genetic basis

13 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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
Literature

Reading

3 publications

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

Request access
09
Provenance

References & sources

8 references

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

Request access