Genopathy
Gene-Disorder Association · Article
Gene
LMNB1
Lamin B1
Disorder
Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant, Typical
First reported 1964
Supporting publications 1
Key publication · disorder [Genetic contribution to the problem of the late form of Pelizaeus-Merzbacher disease].Humangenetik · 1964
Manually curated
Association Review

In brief

The association between LMNB1 (Lamin B1) and Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant, Typical is well established and manually curated, with its 2 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.

Sources 2
Clinical variants 53
Symptoms 112
Compounds 0
Trials 0
Publications 1
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

2 sources

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

Request access
03
LMNB1

The gene

1 source summary

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

Request access
04
Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant, Typical

The disorder

13 database identifiers

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

Request access
05
Phenotype

Clinical features

75 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

53 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

1 publication

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

Request access
09
Provenance

References & sources

7 references

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

Request access