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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
肌萎缩侧索硬化症1型
USH2A c.8559-2A>G
囊性纤维化
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中文
罕见病
Helsmoortel-Van Der Aa Syndrome (HVDAS)
Alias:
Hvdas
Adnp Syndrome
Mrd28
Adnp-Related Multiple Congenital Anomalies - Intellectual Disability - Autism Spectrum Disorder
Adnp-Related Syndromic Intellectual Disability-Autism Spectrum Disorder
Mental Retardation, Autosomal Dominant 28
Adnp-Related Multiple Congenital Anomalies-Intellectual Disability-Autism Spectrum Disorder
Adnp-Related Intellectual Disability and Autism Spectrum Disorder
Mental Retardation, Autosomal Dominant 28, Formerly
Autosomal Dominant Mental Retardation 28
Mrd28, Formerly
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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
Helsmoortel-Van Der Aa 综合症,也被称为 hvdas,与综合智力障碍和自闭症谱系障碍有关。与 Helsmoortel-Van Der Aa 综合症相关的重要基因是 ADNP(活动依赖性神经保护盒),其相关通路/超级通路包括染色体组织和 PKMTs 甲基化组蛋白赖氨酸。在该疾病的背景下提到了药物 Ketamine 和 Anesthetics。附属组织包括心脏和大脑,相关表型为全球发育延迟和延迟的语言和语言发展。
Related ID:
MALACARDS:HLS003
OMIM:615873
MESH:D008607
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
婴儿期
1-9/100000
15
144
13
HLS003
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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