Genopathy
Gene-Disorder Association · Article
Gene
UGT1A9
UDP Glucuronosyltransferase Family 1 Member A9
Disorder
Hyperbilirubinemia, Transient Familial Neonatal
First reported 1963
Supporting publications 33
Key publication · disorder MATERNAL PHENYLKETONURIA. A CAUSE OF MENTAL RETARDATION IN CHILDREN WITHOUT THE METABOLIC DEFECT.The New England journal of medicine · 1963
Manually curated
Association Review

In brief

The association between UGT1A9 (UDP Glucuronosyltransferase Family 1 Member A9) and Hyperbilirubinemia, Transient Familial Neonatal is well established and manually curated, with its 2 contributing sources — 1 of them expert-curated — recording pathogenic and likely-pathogenic variants.

Sources 2
Clinical variants 91
Symptoms 4
Compounds 0
Trials 0
Publications 33
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

2 sources

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

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03
UGT1A9

The gene

1 source summary

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

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04
Hyperbilirubinemia, Transient Familial Neonatal

The disorder

11 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

3 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

91 clinical variants

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

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07
Population genetics

GWAS signals

1 GWAS phenotype

Gene-associated GWAS phenotypes matching the disorder, with best SNP, score, risk-allele frequency and effect size.

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08
Literature

Reading

33 publications

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

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09
Provenance

References & sources

15 references

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

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