Genopathy
Gene-Disorder Association · Article
Gene
LOC110011216
Paired Like Homeobox 2b Polyalanine Repeat Instability Region
Disorder
Central Hypoventilation Syndrome, Congenital, 1
First reported 2000
Supporting publications 6
Key publication · gene–disorder Late-onset central hypoventilation with hypothalamic dysfunction: a distinct clinical syndrome.Pediatric pulmonology · 2000
Key publication · disorder Failure of automatic control of ventilation (Ondine's curse). Report of an infant born with this syndrome and review of the literature.Medicine · 1970
Manually curated
Association Review

In brief

The association between LOC110011216 (Paired Like Homeobox 2b Polyalanine Repeat Instability Region) and Central Hypoventilation Syndrome, Congenital, 1 is well established and manually curated, drawing on a single expert-curated source, which records pathogenic and likely-pathogenic variants.

Sources 1
Clinical variants 19
Symptoms 47
Compounds 0
Trials 0
Publications 6
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
LOC110011216

The gene

1 source summary

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

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04
Central Hypoventilation Syndrome, Congenital, 1

The disorder

16 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

20 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

19 clinical variants

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

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07
Literature

Reading

6 publications

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

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08
Provenance

References & sources

11 references

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

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