Spastic Paraplegia 25, Autosomal Recessive (SPG25)

Alias:
Spg25
Autosomal Recessive Spastic Paraplegia Type 25
Autosomal Recessive Spastic Paraplegia-Disc Herniation Syndrome
Hereditary Spastic Paraplegia 25
Disc Herniation with Spastic Paraplegia, Autosomal Recessive
Autosomal Recessive Spastic Paraplegia 25
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Spastic Paraplegia 25, Autosomal Recessive, also known as spg25, is related to leukodystrophy, hypomyelinating, 11 and leukodystrophy, hypomyelinating, 4, and has symptoms including back pain and neck pain. An important gene associated with Spastic Paraplegia 25, Autosomal Recessive is SPG25 (Spastic Paraplegia 25 (Autosomal Recessive, With Disc Herniation)), and among its related pathways/superpathways is Pyrimidine metabolism. Affiliated tissues include spinal cord and bone, and related phenotypes are paraparesis and herniation of intervertebral nuclei

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Adult
<1/1000000
6
28
1

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!
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