Genopathy
Gene-Disorder Association · Article
Gene
DLL4
Delta Like Canonical Notch Ligand 4
Disorder
Adams-Oliver Syndrome
First reported 2015
Supporting publications 1
Key publication · gene–disorder Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome.American journal of human genetics · 2015
Key publication · disorder Congenital scalp defects with distal limb anomalies: report of a family.Journal of medical genetics · 1976
Manually curated
Association Review

In brief

The association between DLL4 (Delta Like Canonical Notch Ligand 4) and Adams-Oliver 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 9
Symptoms 50
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

3 sources

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

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03
DLL4

The gene

1 source summary

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

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04
Adams-Oliver Syndrome

The disorder

8 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

46 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

9 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

2 shared pathways

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

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08
Literature

Reading

1 publication

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

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09
Provenance

References & sources

12 references

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

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