Autosomal Recessive Ataxia Due to Pex10 Deficiency

Alias:
Mild Peroxisomal Disorder Due to Pex10 Deficiency
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Autosomal Recessive Ataxia Due to Pex10 Deficiency, is also known as mild peroxisomal disorder due to pex10 deficiency. An important gene associated with Autosomal Recessive Ataxia Due to Pex10 Deficiency is PEX10 (Peroxisomal Biogenesis Factor 10). Related phenotypes are motor axonal neuropathy and progressive cerebellar ataxia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Child
<1/1000000
1
6
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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
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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
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IF
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