Genopathy
Gene-Disorder Association · Article
Gene
CYP7B1
Cytochrome P450 Family 7 Subfamily B Member 1
Disorder
Bile Acid Synthesis Defect, Congenital, 3
First reported 1998
Supporting publications 3
Key publication · gene–disorder Identification of a new inborn error in bile acid synthesis: mutation of the oxysterol 7alpha-hydroxylase gene causes severe neonatal liver disease.The Journal of clinical investigation · 1998
Key publication · disorder Familial unconjugated hyperbilirubinemia syndromes.Seminars in liver disease · 1983
Manually curated
Association Review

In brief

The association between CYP7B1 (Cytochrome P450 Family 7 Subfamily B Member 1) and Bile Acid Synthesis Defect, Congenital, 3 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and a causative germline mutation.

Sources 4
Clinical variants 28
Symptoms 37
Compounds 0
Trials 0
Publications 3
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

4 sources

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

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03
CYP7B1

The gene

1 source summary

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

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04
Bile Acid Synthesis Defect, Congenital, 3

The disorder

12 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

24 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

28 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

3 publications

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

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09
Provenance

References & sources

11 references

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

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