Genopathy
Gene-Disorder Association · Article
Gene
ASCL1
Achaete-Scute Family BHLH Transcription Factor 1
Disorder
Central Hypoventilation Syndrome, Congenital, 1
First reported 2003
Supporting publications 1
Key publication · gene–disorder Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse).Human molecular genetics · 2003
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 ASCL1 (Achaete-Scute Family BHLH Transcription Factor 1) and Central Hypoventilation Syndrome, Congenital, 1 is reported, with clinical genetic testing available.

Sources 1
Clinical variants 3
Symptoms 47
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

1 source

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

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03
ASCL1

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

3 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

7 references

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

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