Genopathy
Gene-Disorder Association · Article
Gene
CHD2
Chromodomain Helicase DNA Binding Protein 2
Disorder
Sifrim-Hitz-Weiss Syndrome
First reported 2011
Key publication · disorder Increased exonic de novo mutation rate in individuals with schizophrenia.Nature genetics · 2011
Association Review

In brief

The association between CHD2 (Chromodomain Helicase DNA Binding Protein 2) and Sifrim-Hitz-Weiss Syndrome is supported by expert-curated evidence, drawing on a single expert-curated source, which records pathogenic variants.

Sources 1
Clinical variants 1
Symptoms 71
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.

Request access
02
Provenance

Evidence and sources

1 source

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

Request access
03
CHD2

The gene

1 source summary

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

Request access
04
Sifrim-Hitz-Weiss Syndrome

The disorder

9 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

Request access
05
Phenotype

Clinical features

39 clinical features

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

Request access
06
ClinVar and variant evidence

Genetic basis

1 clinical variant

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

Request access
07
Mechanism overlap

Shared mechanisms

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

Request access
08
Provenance

References & sources

5 references

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

Request access