Neurodevelopmental Disorder with Coarse Facies and Mild Distal Skeletal Abnormalities (NEDCFSA)

Alias:
Nedcfsa
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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
神经发育障碍伴粗糙面容和轻度远端骨骼异常,也称为nedcfsa,与李-弗拉门尼综合症有关。与神经发育障碍伴粗糙面容和轻度远端骨骼异常有关的重要基因是KDM6B(赖氨酸去甲基酶6B)。附属组织包括心脏,相关表型为语言发育延迟和运动延迟。
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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未知
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Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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No data available

Related Drugs

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No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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No Data Found!
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