Developmental and Epileptic Encephalopathy 76 (DEE76)

Alias:
Epileptic Encephalopathy, Early Infantile, 76
Dee76
Developmental and Epileptic Encephalopathy, 76
Eiee76
Decam
Developmental Delay, Epileptic Encephalopathy, Cerebral Atrophy, and Abnormal Myelination
Developmental Delay, Epileptic Endephalopathy, Cerebral Atrophy, and Abnormal Myelination
Early Infantile Epileptic Encephalopathy 76
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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
发育性和癫痫性脑病76,也称为癫痫性脑病,早期婴儿型76,与小脑萎缩、发育迟缓和癫痫发作和脑萎缩有关。与发育性和癫痫性脑病76有关的重要基因是ACTL6B(Actin Like 6B),其相关通路/超级通路包括Rett综合征致病基因和RUNX1与尚不清楚其精确效果的共因子相互作用。附属组织包括大脑和眼睛,相关表型为智力障碍和癫痫发作。
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
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13
73
5

Medical Symptom

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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

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CAS Number
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Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
No Data Found!
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