Leukodystrophy, Hypomyelinating, 5 (HLD5)

Alias:
Hypomyelination and Congenital Cataract
Hypomyelination-Congenital Cataract Syndrome
Hld5
Hypomyelinating Leukodystrophy 5
Hcc
Hypomyelination and Congenital Cataract: Hcc
Hypomyelination with Congenital Cataract
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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,5型,也称为白质营养不良和先天性白内障,与痉挛和白质营养不良有关,症状包括异常锥体征、动作震颤和小脑征。与白质营养不良症,5型有关的重要基因是HYCC1(Hyccin PI4KA脂质激酶复合物亚基1),其相关通路/超级通路包括少突胶质细胞特化和分化,导致中枢神经系统髓鞘成分和小胶质细胞分化。附属组织包括眼睛和大脑,相关表型为异常锥体征和全球发育延迟。
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
<1/1000000
19
162
11

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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