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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
罕见病
Pitt-Hopkins-Like Syndrome 1 (PTHSL1)
Alias:
Cortical Dysplasia-Focal Epilepsy Syndrome
Cdfes
Cdfe Syndrome
Pthsl1
Pitt-Hopkins Like Syndrome 1
Cntnap2-Related Developmental and Epileptic Encephalopathy
Pitt-Hopkins-Like Syndrome-1
Cntnap2-Related Dee
Mesh; D006985
Mesh; D008607
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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
Pitt-Hopkins-Like Syndrome 1,也被称为皮特-霍普金斯类似症候群1,与皮特-霍普金斯类似症候群2和皮特-霍普金斯症候群有关。与Pitt-Hopkins-Like Syndrome 1相关的基因是CNTNAP2(接触蛋白关联蛋白2),其相关通路/超级通路包括化学突触间的传递和神经科学。相关组织包括大脑和眼睛,相关表型包括癫痫和语言发育延迟。
Related ID:
MALACARDS:PTT029
OMIM:610042
MESH:C567657
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
婴儿期
--
22
262
21
PTT029
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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