Genopathy
Gene-Disorder Association · Article
Gene
GALT
Galactose-1-Phosphate Uridylyltransferase
Disorder
Cataract
First reported 1990
Supporting publications 5
Key publication · gene–disorder [Identification of inborn errors of galactose metabolism in patients with cataracts].Archivos de investigacion medica · 1990
Key publication · disorder Hereditary congenital spinocerebellar ataxia accompanied by congenital cataract and oligophrenia; a genetic and clinical investigation.Confinia neurologica · 1950
Manually curated
Association Review

In brief

The association between GALT (Galactose-1-Phosphate Uridylyltransferase) and Cataract is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 0
Compounds 0
Trials 0
Publications 5
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
GALT

The gene

1 source summary

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

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04
Cataract

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
Literature

Reading

5 publications

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

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06
Provenance

References & sources

7 references

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

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