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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
Hereditary Optic Neuropathy
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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
遗传性视神经病变与Leber视神经萎缩、肌张力障碍和伴有或不伴有听神经病变的视神经萎缩有关。与遗传性视神经病变有关的重要基因是MT-ND4(线粒体编码的NADH:泛醌氧化还原酶核心亚基4),其相关通路/超级通路包括代谢和呼吸电子传递、化学耦联ATP合成和解耦联蛋白产生的热量。在该疾病的背景下提到了Idebenone和抗氧化剂。附属组织包括眼睛和骨髓。
Related ID:
MALACARDS:HRD217
ICD11:2452831
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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未知
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HRD217
Medical Symptom
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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
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IF
No Data Found!
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