Pontocerebellar Hypoplasia, Type 2a (PCH2A)

Alias:
Pontocerebellar Hypoplasia Type 2a
Pontocerebellar Hypoplasia with Progressive Cerebral Atrophy
Volendam Neurodegenerative Disease
Pch2a
Pch2
Hypoplasia, Pontocerebellar, Type 2a
Pontocerebellar Hypoplasia 2a
Favorite
Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Pontocerebellar Hypoplasia, Type 2a, also known as pontocerebellar hypoplasia type 2a, is related to pontocerebellar hypoplasia, type 2e and pontocerebellar hypoplasia, type 2f, and has symptoms including muscle spasticity, seizures and opisthotonus. An important gene associated with Pontocerebellar Hypoplasia, Type 2a is TSEN54 (TRNA Splicing Endonuclease Subunit 54), and among its related pathways/superpathways are RNA Polymerase III Transcription Initiation and tRNA processing. Affiliated tissues include spinal cord and cerebellum, and related phenotypes are cerebral cortical atrophy and progressive microcephaly
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
7
31
17

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