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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
非罕见病
Neurodevelopmental Disorder with Spastic Diplegia and Visual Defects (NEDSDV)
Alias:
Nedsdv
Severe Intellectual Disability-Progressive Spastic Diplegia Syndrome
Eurodevelopmental Disorder with Spastic Diplegia and Visual Defects
Mental Retardation, Autosomal Dominant 19, Formerly
Mrd19, Formerly
Mrd19
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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
神经发育障碍伴痉挛性截瘫和视觉缺陷,也称为nedsdv,与严重的智力障碍-进行性痉挛性截瘫综合征和常染色体显性智力发育障碍19有关。与神经发育障碍伴痉挛性截瘫和视觉缺陷有关的重要基因是CTNNB1(β-连环蛋白)。附属组织包括皮肤和大脑,相关表型为智力障碍和全球发育延迟。
Related ID:
MALACARDS:NRD057
OMIM:615075
MESH:D008607
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
未知
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1
31
14
NRD057
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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