Genopathy
Gene-Disorder Association · Article
Gene
RAB32
RAB32, Member RAS Oncogene Family
Disorder
Parkinson Disease 26, Autosomal Dominant
First reported 2000
Key publication · disorder Autosomal recessive early-onset parkinsonism with diurnal fluctuation: clinicopathologic characteristics and molecular genetic identification.Brain & development · 2000
Manually curated
Association Review

In brief

The association between RAB32 (RAB32, Member RAS Oncogene Family) and Parkinson Disease 26, Autosomal Dominant is a manually-curated gene–disease association, drawing on a single expert-curated source, which records a known molecular basis and a susceptibility locus.

Sources 1
Clinical variants 0
Symptoms 44
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
RAB32

The gene

1 source summary

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

Request access
04
Parkinson Disease 26, Autosomal Dominant

The disorder

6 database identifiers

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

Request access
05
Phenotype

Clinical features

41 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

3 references

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

Request access