Parkinson Disease 2, Autosomal Recessive Juvenile (PARK2)

Alias:
Autosomal Recessive Juvenile Parkinson Disease 2
Parkinsonism, Early-Onset, with Diurnal Fluctuation
Parkinson Disease, Juvenile, Autosomal Recessive
Parkinson Disease, Juvenile, Type 2
Parkinson's Disease 2
Parkinson Disease 2
Park2
Epdf
Pdj
Autosomal Recessive Early-Onset Parkinson Disease Type 2
Chromosome 6-Linked Autosomal Recessive Parkinsonism
Autosomal Recessive Juvenile Parkinson's Disease 2
Early-Onset Parkinsonism with Diurnal Fluctuation
Autosomal Recessive Juvenile Parkinson Disease
Parkinsonism Young Adult Onset
Parkinson Disease, Type 2
Parkinsonism, Juvenile
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Parkinson Disease 2, Autosomal Recessive Juvenile, also known as autosomal recessive juvenile parkinson disease 2, is related to early-onset parkinson's disease and young-onset parkinson disease, and has symptoms including muscle rigidity, tremor and bradykinesia. An important gene associated with Parkinson Disease 2, Autosomal Recessive Juvenile is PRKN (Parkin RBR E3 Ubiquitin Protein Ligase), and among its related pathways/superpathways are DNA Damage and Mitophagy. Affiliated tissues include brain and cortex, and related phenotypes are tremor and parkinsonism
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Adult
--
11
72
100

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Mutations
No data available

Related Drugs

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Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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