Genopathy
Gene-Disorder Association · Article
Gene
MBS3
Moebius Syndrome 3
Disorder
Facial Paresis, Hereditary Congenital, 2
First reported 1986
Key publication · disorder Hereditary congenital facial paralysis.Scandinavian journal of plastic and reconstructive surgery · 1986
Manually curated
Association Review

In brief

The association between MBS3 (Moebius Syndrome 3) and Facial Paresis, Hereditary Congenital, 2 is a manually-curated gene–disease association, supported by a single expert-curated source.

Sources 1
Clinical variants 0
Symptoms 5
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
Facial Paresis, Hereditary Congenital, 2

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

2 clinical features

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

Request access
05
Provenance

References & sources

2 references

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

Request access