Genopathy
Gene-Disorder Association · Article
Gene
CIB2
Calcium And Integrin Binding Family Member 2
Disorder
Leber Plus Disease
First reported 1951
Key publication · disorder [Familial retrobulbar optic neuritis (Leber's disease)].Annali di medicina navale · 1951
Manually curated
Association Review

In brief

The association between CIB2 (Calcium And Integrin Binding Family Member 2) and Leber Plus Disease is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 29
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
CIB2

The gene

1 source summary

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

Request access
04
Leber Plus Disease

The disorder

17 database identifiers

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

Request access
05
Phenotype

Clinical features

25 clinical features

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

Request access
06
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

Request access
07
Provenance

References & sources

6 references

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

Request access