Genopathy
Gene-Disorder Association · Article
Gene
LEMD3
LEM Domain Containing 3
Disorder
Buschke-Ollendorff Syndrome
First reported 2004
Supporting publications 10
Key publication · gene–disorder Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis.Nature genetics · 2004
Key publication · disorder Osteopoikilosis (osteopathia condensans disseminata).Chirurgia narzadow ruchu i ortopedia polska · 1953
Manually curated
Association Review

In brief

The association between LEMD3 (LEM Domain Containing 3) and Buschke-Ollendorff Syndrome is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.

Sources 3
Clinical variants 104
Symptoms 19
Compounds 0
Trials 0
Publications 10
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
LEMD3

The gene

1 source summary

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

Request access
04
Buschke-Ollendorff Syndrome

The disorder

12 database identifiers

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

Request access
05
Phenotype

Clinical features

11 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

104 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

10 publications

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

Request access
09
Provenance

References & sources

14 references

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

Request access