Spinocerebellar Ataxia 49 (SCA49)

Alias:
Sca49
Ataxia, Spinocerebellar, Type 49
Spinocerebellar Ataxia Type 49
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Spinocerebellar Ataxia 49, also known as sca49, is related to aceruloplasminemia and polyneuropathy. An important gene associated with Spinocerebellar Ataxia 49 is SAMD9L (Sterile Alpha Motif Domain Containing 9 Like). Affiliated tissues include spinal cord and cerebellum, and related phenotypes are hyperreflexia and cerebellar atrophy
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
--
1
6
2

Medical Symptom

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

Gene & Mutation

#
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

Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Tutorials
Back to top