Spastic Paraplegia 91, Autosomal Dominant, with or Without Cerebellar Ataxia (SPG91)

Alias:
Spg91
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Spastic Paraplegia 91, Autosomal Dominant, with or Without Cerebellar Ataxia, also known as spg91, is related to developmental delay with or without epilepsy. An important gene associated with Spastic Paraplegia 91, Autosomal Dominant, with or Without Cerebellar Ataxia is SPTAN1 (Spectrin Alpha, Non-Erythrocytic 1). Affiliated tissues include brain and eye.

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
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