Neurodevelopmental Disorder with Hypotonia, Dysmorphic Facies, and Skin Abnormalities (NEDHFS)

Alias:
Nedhfs
Neurodevelopmental Disorder with Hypotonia, Dysmorphic Facies, Skin Abnormalities
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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、畸形面容和皮肤异常,也称为nedhfs。与神经发育障碍伴低张力、畸形面容和皮肤异常有关的重要基因是PGM2L1(磷酸葡萄糖变位酶2类似物1)。相关组织包括皮肤和大脑,相关表型为智力障碍和全球发育延迟。
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
未知
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1
2
1

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
Status
Phase
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
Journal
Year
IF
No Data Found!
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