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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
Neurodevelopmental Disorder with Neonatal Respiratory Insufficiency, Hypotonia, and Feeding Difficulties (NEDRIHF)
Alias:
Pura-Related Severe Neonatal Hypotonia-Seizures-Encephalopathy Syndrome Due to a Point Mutation
Nedrihf
Pura-Related Severe Neonatal Hypotonia-Seizures-Encephalopathy Syndrome
Mental Retardation, Autosomal Dominant 31, Formerly
Mrd31, Formerly
Mrd31
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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
神经发育障碍伴新生儿呼吸不足、肌张力低下和喂养困难,也称为点突变引起的pura相关严重新生儿肌张力低下-惊厥-脑病综合征,与pura综合征和常染色体显性智力发育障碍31有关。与神经发育障碍伴新生儿呼吸不足、肌张力低下和喂养困难有关的重要基因是PURA(富含嘌呤元素结合蛋白A)。相关组织包括大脑和心脏,相关表型为惊厥和全球发育延迟。
Related ID:
MALACARDS:NRD129
OMIM:616158
MESH:D008607
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
新生儿
<1/1000000
1
5
22
NRD129
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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