Genopathy
Gene-Disorder Association · Article
Gene
ALDH18A1
Aldehyde Dehydrogenase 18 Family Member A1
Disorder
Autosomal Recessive Cutis Laxa Type Iii
First reported 1974
Supporting publications 21
Key publication · disorder [De Barsy syndrome, a further case (author's transl)].Klinische Padiatrie · 1974
Association Review

In brief

The association between ALDH18A1 (Aldehyde Dehydrogenase 18 Family Member A1) and Autosomal Recessive Cutis Laxa Type Iii is supported by expert-curated evidence, drawing on a single expert-curated source, which records likely-pathogenic variants.

Sources 1
Clinical variants 535
Symptoms 69
Compounds 0
Trials 0
Publications 21
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
ALDH18A1

The gene

1 source summary

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

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04
Autosomal Recessive Cutis Laxa Type Iii

The disorder

8 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

66 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

535 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

21 publications

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

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09
Provenance

References & sources

14 references

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

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