Genopathy
Gene-Disorder Association · Article
Gene
EFEMP2
EGF-Like Fibulin Extracellular Matrix Protein 2
Disorder
Cutis Laxa, Autosomal Recessive, Type Ib
First reported 2013
Supporting publications 21
Key publication · gene–disorder Longer term survival of a child with autosomal recessive cutis laxa due to a mutation in FBLN4.American journal of medical genetics. Part A · 2013
Key publication · disorder Comparison of intravenous and topical lidocaine as a suppressant of coughing after bronchoscopy during general anesthesia.Acta anaesthesiologica Scandinavica · 1991
Manually curated
Association Review

In brief

The association between EFEMP2 (EGF-Like Fibulin Extracellular Matrix Protein 2) and Cutis Laxa, Autosomal Recessive, Type Ib is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and causative variation.

Sources 4
Clinical variants 394
Symptoms 79
Compounds 0
Trials 0
Publications 21
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

4 sources

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

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03
EFEMP2

The gene

1 source summary

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

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04
Cutis Laxa, Autosomal Recessive, Type Ib

The disorder

9 database identifiers

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

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05
Phenotype

Clinical features

47 clinical features

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

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06
ClinVar and variant evidence

Genetic basis

394 clinical variants

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

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07
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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08
Literature

Reading

21 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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