Genopathy
Gene-Disorder Association · Article
Gene
CYP1B1
Cytochrome P450 Family 1 Subfamily B Member 1
Disorder
Juvenile Glaucoma
First reported 2011
Supporting publications 12
Key publication · gene–disorder CYP1B1-related anterior segment developmental anomalies novel mutations for infantile glaucoma and von Hippel's ulcer revisited.Ophthalmology · 2011
Key publication · disorder [Hydrophthalmos associated with facial nevus].Revista brasileira de oftalmologia · 1950
Manually curated
Association Review

In brief

The association between CYP1B1 (Cytochrome P450 Family 1 Subfamily B Member 1) and Juvenile Glaucoma is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic variants and a susceptibility locus.

Sources 3
Clinical variants 1
Symptoms 16
Compounds 0
Trials 0
Publications 12
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

3 sources

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

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03
CYP1B1

The gene

2 source summaries

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

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04
Juvenile Glaucoma

The disorder

7 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

15 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

1 clinical variant

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

12 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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