Progressive Bulbar Palsy

Alias:
Bulbar Palsy, Progressive
Pbp - [progressive Bulbar Palsy]
Supranuclear Bulbar Paralysis
Progressive Bulbar Paralysis
Chronic Bulbar Paralysis
Chronic Bulbar Palsy
Bulbar Paralysis
Bulbar Palsy
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Progressive Bulbar Palsy, also known as bulbar palsy, progressive, is related to brown-vialetto-van laere syndrome 1 and fazio-londe disease. An important gene associated with Progressive Bulbar Palsy is SLC52A3 (Solute Carrier Family 52 Member 3), and among its related pathways/superpathways are Metabolism and Metabolism of water-soluble vitamins and cofactors. Affiliated tissues include spinal cord and tongue, and related phenotypes are behavior/neurological and mortality/aging
Related ID:
MESH:D010244
ICD11:1143049440

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Unknown
--
18
154
--

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