Parkinson Disease 22, Autosomal Dominant (PARK22)

Alias:
Parkinson's Disease 22
Park22
Autosomal Dominant Parkinson's Disease 22
Parkinson Disease 22
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Parkinson Disease 22, Autosomal Dominant, also known as parkinson's disease 22, is related to parkinson disease, late-onset and avian influenza. An important gene associated with Parkinson Disease 22, Autosomal Dominant is CHCHD2 (Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing 2). Affiliated tissues include brain and cortex, and related phenotypes are gait disturbance and rigidity
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
--
3
30
4

Medical Symptom

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

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
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
Journal
Year
IF
No Data Found!
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