Genopathy
Gene-Disorder Association · Article
Gene
TGFB3
Transforming Growth Factor Beta 3
Disorder
Epilepsy, Myoclonic Juvenile
First reported 1970
Key publication · disorder [Genetic study of a family with juvenile myoclonus-epilepsy with cherry red spots in the fundus oculi].Bollettino della Societa italiana di biologia sperimentale · 1970
Manually curated
Association Review

In brief

The association between TGFB3 (Transforming Growth Factor Beta 3) and Epilepsy, Myoclonic Juvenile is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 23
Compounds 0
Trials 0
Publications 0
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
TGFB3

The gene

1 source summary

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

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04
Epilepsy, Myoclonic Juvenile

The disorder

13 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

14 clinical features

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

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06
Provenance

References & sources

7 references

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

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