Genopathy
Gene-Disorder Association · Article
Gene
FBLN7
Fibulin 7
Disorder
2q13 Microdeletion Syndrome
First reported 2016
Supporting publications 1
Key publication · disorder Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital heart disease and restrictive cardiomyopathy.Cold Spring Harbor molecular case studies · 2016
Manually curated
Association Review

In brief

The association between FBLN7 (Fibulin 7) and 2q13 Microdeletion Syndrome is a manually-curated gene–disease association, supported by a single expert-curated source.

Sources 1
Clinical variants 0
Symptoms 0
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.

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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
FBLN7

The gene

1 source summary

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

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04
2q13 Microdeletion Syndrome

The disorder

4 database identifiers

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

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05
Literature

Reading

1 publication

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

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06
Provenance

References & sources

3 references

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

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