Genopathy
Gene-Disorder Association · Article
Gene
DCC
DCC Netrin 1 Receptor
Disorder
Gaze Palsy, Familial Horizontal, With Progressive Scoliosis 2, With Impaired Intellectual Development
First reported 2017
Supporting publications 1
Key publication · gene–disorder Biallelic mutations in human DCC cause developmental split-brain syndrome.Nature genetics · 2017
Key publication · disorder Horizontal gaze palsy with progressive scoliosis in a Moroccan family.Orthopaedics & traumatology, surgery & research : OTSR · 2014
Manually curated
Association Review

In brief

The association between DCC (DCC Netrin 1 Receptor) and Gaze Palsy, Familial Horizontal, With Progressive Scoliosis 2, With Impaired Intellectual Development is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.

Sources 3
Clinical variants 16
Symptoms 32
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
DCC

The gene

1 source summary

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

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04
Gaze Palsy, Familial Horizontal, With Progressive Scoliosis 2, With Impaired Intellectual Development

The disorder

7 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

19 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

16 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

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

6 references

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

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