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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
Retinal Dystrophy with Leukodystrophy (RDLKD)
Alias:
Rdlkd
Dystrophy, Retinal, with Leukodystrophy
Acbd5 Deficiency
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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
视网膜营养不良伴白质营养不良,也称为rdlkd,与白质营养不良和过氧化物酶体疾病有关。与视网膜营养不良伴白质营养不良相关的基因是ACBD5(酰基辅酶A结合域含5),其相关通路/超通路包括代谢和脂肪酸代谢。附属组织包括脑桥,相关表型为运动性构音障碍和语言发育延迟。
Related ID:
MALACARDS:RTN231
OMIM:618863
MESH:D020279
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
--
15
71
3
RTN231
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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