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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
Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant (ADLD)
Alias:
Adult-Onset Autosomal Dominant Demyelinating Leukodystrophy
Adld
Leukodystrophy, Adult-Onset, Autosomal Dominant
Adult-Onset Autosomal Dominant Leukodystrophy
Pelizaeus-Merzbacher Disease, Autosomal Dominant or Late-Onset Type, Formerly
Autosomal-Dominant or Late-Onset Type Pelizaeus-Merzbacher Disease
Leukodystrophy, Demyelinating, Autosomal Dominant, Adult-Onset
Pelizaeus-Merzbacher Disease Autosomal Dominant
Adult Onset Autosomal Dominant Leukodystrophy
Pelizaeus-Merzbacher Disease Late-Onset Type
Multiple Sclerosis-Like Disorder
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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
白质营养不良症,脱髓鞘型,成人型,常染色体显性遗传,也称为成人型常染色体显性脱髓鞘白质营养不良症,与常染色体显性白质营养不良伴自主神经病和LMNB1相关常染色体显性白质营养不良有关,症状包括小脑共济失调、肌肉痉挛和异常锥体征。与白质营养不良症,脱髓鞘型,成人型,常染色体显性遗传相关的基因是LMNB1(Lamin B1),其相关通路/超级通路包括DREAM抑制和杜氏醇表达和细胞骨架信号传导。相关组织包括眼睛和脊髓,相关表型为共济失调和自主神经系统生理异常。
Related ID:
MALACARDS:LKD025
OMIM:169500
MESH:D020279
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
成年期
--
17
137
20
LKD025
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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