Genopathy
Gene-Disorder Association · Article
Gene
FBLN5
Fibulin 5
Disorder
Cutis Laxa
First reported 2002
Supporting publications 11
Key publication · gene–disorder Homozygosity for a missense mutation in fibulin-5 (FBLN5) results in a severe form of cutis laxa.Human molecular genetics · 2002
Key publication · disorder [Cutis laxa].Archiv fur Dermatologie und Syphilis · 1951
Manually curated
Association Review

In brief

The association between FBLN5 (Fibulin 5) and Cutis Laxa is reported, with clinical genetic testing available.

Sources 1
Clinical variants 54
Symptoms 1
Compounds 0
Trials 0
Publications 11
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

1 source

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

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03
FBLN5

The gene

1 source summary

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

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04
Cutis Laxa

The disorder

10 database identifiers

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

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05
ClinVar and variant evidence

Genetic basis

54 clinical variants

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

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06
Literature

Reading

11 publications

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

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07
Provenance

References & sources

13 references

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

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