Genopathy
Gene-Disorder Association · Article
Gene
SETD5
SET Domain Containing 5
Disorder
3p25.3 Microdeletion Syndrome
First reported 2024
Supporting publications 1
Key publication · disorder Interstitial 3p25.3 deletion syndrome: 13 years'-long follow-up of an affected individual.Clinical dysmorphology · 2024
Manually curated
Association Review

In brief

The association between SETD5 (SET Domain Containing 5) and 3p25.3 Microdeletion Syndrome is a manually-curated gene–disease association, supported by a single expert-curated source.

Sources 1
Clinical variants 0
Symptoms 55
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
SETD5

The gene

1 source summary

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

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04
3p25.3 Microdeletion Syndrome

The disorder

5 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

51 clinical features

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

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06
Mechanism overlap

Shared mechanisms

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

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07
Literature

Reading

1 publication

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

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08
Provenance

References & sources

5 references

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

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