Genopathy
Gene-Disorder Association · Article
Gene
TGFBR2
Transforming Growth Factor Beta Receptor 2
Disorder
Loeys-Dietz Syndrome
First reported 2005
Supporting publications 22
Key publication · gene–disorder Identification of a novel TGFBR2 gene mutation in a Korean patient with Loeys-Dietz aortic aneurysm syndrome; no mutation in TGFBR2 gene in 30 patients with classic Marfan's syndrome.Clinical genetics · 2005
Key publication · disorder Two-dimensional echocardiographic aortic root dimensions in normal children and adults.The American journal of cardiology · 1989
Manually curated
Association Review

In brief

The association between TGFBR2 (Transforming Growth Factor Beta Receptor 2) and Loeys-Dietz Syndrome is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.

Sources 3
Clinical variants 106
Symptoms 38
Compounds 0
Trials 0
Publications 22
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

3 sources

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

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03
TGFBR2

The gene

1 source summary

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

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04
Loeys-Dietz Syndrome

The disorder

11 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

37 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

106 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

1 shared pathway

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

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08
Literature

Reading

22 publications

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

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09
Provenance

References & sources

15 references

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

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