Genopathy
Gene-Disorder Association · Article
Gene
PCDHGC4
Protocadherin Gamma Subfamily C, 4
Disorder
Neurodevelopmental Disorder With Poor Growth And Skeletal Anomalies
First reported 1993
Supporting publications 1
Key publication · disorder Costello syndrome: further clinical delineation, natural history, genetic definition, and nosology.American journal of medical genetics · 1993
Manually curated
Association Review

In brief

The association between PCDHGC4 (Protocadherin Gamma Subfamily C, 4) and Neurodevelopmental Disorder With Poor Growth And Skeletal Anomalies is well established and manually curated, with its 2 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.

Sources 2
Clinical variants 9
Symptoms 63
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

2 sources

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

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03
PCDHGC4

The gene

1 source summary

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

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04
Neurodevelopmental Disorder With Poor Growth And Skeletal Anomalies

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

29 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

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

5 references

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

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