Neurodevelopmental Disorder with Hypotonia, Dysmorphic Facies, and Skeletal Anomalies, with or Without Seizures (NEDFSS)

Alias:
Nedfss
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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
神经发育障碍伴低张力、畸形面容和骨骼异常,伴有或不伴有癫痫,也称为nedfss。与神经发育障碍伴低张力、畸形面容和骨骼异常,伴有或不伴有癫痫有关的重要基因是TRPM3(瞬时受体电位阳离子通道家族M成员3)。相关组织包括大脑和眼睛,相关表型包括智力障碍和癫痫。
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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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1
7
7

Medical Symptom

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

Gene & Mutation

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Score
Mutations
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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PMID
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IF
No Data Found!
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