Pontocerebellar Hypoplasia, Type 2d (PCH2D)

Alias:
Pontocerebellar Hypoplasia Type 2d
Pcca
Progressive Cerebello-Cerebral Atrophy
Pch2d
Cerebellocerebral Atrophy, Progressive
Progressive Cerebellocerebral Atrophy
Hypoplasia, Pontocerebellar, Type 2d
Pontocerebellar Hypoplasia 2d
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基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
桥脑小脑发育不全2d型,也称为桥脑小脑发育不全2d型,与桥脑小脑发育不全2e和四肢瘫痪有关,症状包括抽搐、癫痫和睡眠障碍。与桥脑小脑发育不全2d型有关的重要基因是SEPSECS(Sep(O-磷酸丝氨酸)tRNA:Sec(硒代半胱氨酸)tRNA合成酶),其相关通路/超级通路包括活性氧清除、硒代谢和硒蛋白。相关组织包括大脑和小脑,相关表型为癫痫和全球发育迟缓。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
<1/1000000
16
94
4

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
No Data Found!
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