Developmental and Epileptic Encephalopathy 25 (DEE25)

Alias:
Developmental and Epileptic Encephalopathy, 25
Developmental and Epileptic Encephalopathy 25, with Amelogenesis Imperfecta
Early Infantile Epileptic Encephalopathy 25
Dee25
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Developmental and Epileptic Encephalopathy 25, also known as developmental and epileptic encephalopathy, 25, is related to developmental and epileptic encephalopathy 25 with amelogenesis imperfecta and kohlschutter-tonz syndrome, and has symptoms including ataxia, muscle spasticity and tonic seizures. An important gene associated with Developmental and Epileptic Encephalopathy 25 is SLC13A5 (Solute Carrier Family 13 Member 5), and among its related pathways/superpathways is Transport of inorganic cations/anions and amino acids/oligopeptides. The drugs Sodium citrate and Citric acid have been mentioned in the context of this disorder. Affiliated tissues include brain, and related phenotype is skeleton.
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Unknown
--
10
58
14

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