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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
Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 2 (CADASIL2)
Alias:
Htra1-Related Autosomal Dominant Cerebral Small Vessel Disease
Cadasil 2
Cadasil2
Autosomal Dominant Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Type 2
Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, 2
Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy, Autosomal Dominant, 2
Htra1-Related Autosomal Dominant Cerebral Angiopathy
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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
大脑动脉病,常染色体显性,伴有皮质下梗死和白质脑病,类型2,也称为htra1相关常染色体显性大脑小血管疾病,与脊柱炎和假性球麻痹有关。与大脑动脉病,常染色体显性,伴有皮质下梗死和白质脑病,类型2相关的基因是HTRA1(HtrA丝氨酸肽酶1),其相关通路/超级通路包括胶原链三聚体化和细胞外基质组织。相关组织包括大脑,相关表型是MRI上大脑白质的高信号和腔隙性脑梗死。
Related ID:
MALACARDS:CRB170
OMIM:616779
MESH:D046589
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
成年期
<1/1000000
16
183
7
CRB170
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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