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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
Leukodystrophy, Hypomyelinating, 23, with Ataxia, Deafness, Liver Dysfunction, and Dilated Cardiomyopathy (HLD23)
Alias:
Hld23
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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23型,伴有共济失调、耳聋、肝功能障碍和扩张型心肌病,也称为hld23,与脱髓鞘型白质营养不良症23型有关。与白质营养不良症,脱髓鞘型23型,伴有共济失调、耳聋、肝功能障碍和扩张型心肌病相关的基因是RNF220(环指蛋白220)。相关组织包括肝脏和大脑,相关表型为高反射性和共济失调。
Related ID:
MALACARDS:LKD036
OMIM:619688
MESH:D020279
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
--
1
7
3
LKD036
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
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Gene
Function
Score
Mutations
No data available
Related Drugs
Name
CAS Number
Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
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Publications
No data available
References Literature
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No Data Found!
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