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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
Intellectual Developmental Disorder, Autosomal Dominant 44, with Microcephaly (MRD44)
Alias:
Micrognathia-Recurrent Infections-Behavioral Abnormalities-Mild Intellectual Disability Syndrome
Mrd44
Autosomal Dominant Intellectual Developmental Disorder 44
Autosomal Dominant Intellectual Developmental Disorder 44 with Microcephaly
Autosomal Dominant Non-Syndromic Intellectual Disability 44
Mental Retardation, Autosomal Dominant, Type 44
Mental Retardation, Autosomal Dominant 44
Autosomal Dominant Mental Retardation 44
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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
智力发育障碍,常染色体显性44型,伴有小头畸形,也称为小颌-反复感染-行为异常-轻度智力障碍综合征,与神经病,遗传性感觉和自主神经,类型IIb和遗传性感觉神经病有关。与智力发育障碍,常染色体显性44型,伴有小头畸形有关的重要基因是TRIO(Trio Rho鸟苷酸交换因子),其相关通路/超级通路包括Netrin-1信号通路。附属组织包括大脑,相关表型为全球发育延迟和轻度智力障碍。
Related ID:
MALACARDS:INT373
OMIM:617061
MESH:D008607
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
新生儿
<1/1000000
8
42
7
INT373
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
#
Gene
Function
Score
Mutations
No data available
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Name
CAS Number
Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
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No data available
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IF
No Data Found!
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