Spinocerebellar Ataxia 36 (SCA36)

Alias:
Spinocerebellar Ataxia Type 36
Sca36
Ataxia, Spinocerebellar, Type 36
Costa De Morte Ataxia
Asidan Ataxia
Asidan
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Spinocerebellar Ataxia 36, also known as spinocerebellar ataxia type 36, is related to olivopontocerebellar atrophy and lateral sclerosis, and has symptoms including cerebellar ataxia and gait ataxia. An important gene associated with Spinocerebellar Ataxia 36 is NOP56 (NOP56 Ribonucleoprotein). Affiliated tissues include tongue and spinal cord, and related phenotypes are ataxia and dysarthria
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Adult
--
18
140
3

Medical Symptom

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

Gene & Mutation

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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
Journal
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IF
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