Neuronal Ceroid Lipofuscinosis (NCL)

Alias:
Hereditary Ceroid Lipofuscinosis
Neuronal Ceroid-Lipofuscinoses
Ncl
Pigmentary Retinal Lipoid Neuronal Heredodegeneration
Juvenile Neuronal Ceroid Lipofuscinosis
Ncl - [neuronal Ceroid Lipofuscinosis]
Lipofuscinosis, Ceroid, Neuronal
Cerebromacular Degeneration
Amaurotic Familial Idiocy
Cerebromacular Dystrophy
Neuronal Lipofuscinosis
Ceroid-Lipofuscinosis
Amaurotic Idiocy
Amaurotic Idiot
Batten Disease
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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
神经性蜡样脂褐质沉积症,也称为遗传性蜡样脂褐质沉积症,与蜡样脂褐质沉积症,神经性,3和蜡样脂褐质沉积症,神经性,10有关,症状包括肌阵挛、癫痫发作和外周运动功能异常。与神经性蜡样脂褐质沉积症有关的重要基因是CLN3(CLN3溶酶体/内体跨膜蛋白,贝特宁)。在该疾病的背景下,已提到的药物包括半胱氨酸和乙酰半胱氨酸。相关组织包括视网膜和大脑,相关表型为神经系统和稳态/代谢
Related ID:
MESH:D009472
ICD11:1568332253

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
常显
全年龄段
1-9/100000
128
1241
230

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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