Genopathy
Gene-Disorder Association · Article
Gene
GLC3B
Glaucoma 3, Primary Infantile, B
Disorder
Glaucoma 3, Primary Infantile, B
First reported 1975
Key publication · disorder Ocular findings and corticosteroid responsiveness in parents of children with primary infantile glaucoma.Investigative ophthalmology · 1975
Manually curated
Association Review

In brief

The association between GLC3B (Glaucoma 3, Primary Infantile, B) and Glaucoma 3, Primary Infantile, B is a manually-curated gene–disease association, supported by a single expert-curated source.

Sources 1
Clinical variants 0
Symptoms 1
Compounds 0
Trials 0
Publications 0
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Request access
02
Provenance

Evidence and sources

1 source

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

Request access
03
Glaucoma 3, Primary Infantile, B

The disorder

5 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

Request access
04
Phenotype

Clinical features

1 clinical feature

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

Request access
05
Provenance

References & sources

1 reference

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

Request access