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Cerebellar Hyplasia/atrophy, Epilepsy, and Global Developmental Delay

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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cerebellar Hyplasia/atrophy, Epilepsy, and Global Developmental Delay An important gene associated with Cerebellar Hyplasia/atrophy, Epilepsy, and Global Developmental Delay is OXR1 (Oxidation Resistance 1).
Related ID：
MALACARDS：CRB216

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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1
7
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CRB216

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

Name
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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Journal
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IF
No Data Found!
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