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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
Houge-Janssens Syndrome 1 (HJS1)
Alias:
Intellectual Disability-Macrocephaly-Hypotonia-Behavioral Abnormalities Syndrome
Mrd35
Intellectual Developmental Disorder, Autosomal Dominant 35
Autosomal Dominant Intellectual Developmental Disorder 35
Autosomal Dominant Non-Syndromic Intellectual Disability 35
Mental Retardation, Autosomal Dominant, Type 35
Mental Retardation, Autosomal Dominant 35
Autosomal Dominant Mental Retardation 35
Hjs1
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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
Houge-Janssens Syndrome 1,又称智力障碍-巨脑-肌张力减退-行为异常综合征,与ppp2r5d相关智力障碍和Houge-Janssens Syndrome 2有关。Houge-Janssens Syndrome 1的一个重要基因是PPP2R5D(蛋白磷酸酶2调节亚基B'Delta),其相关通路/超级通路包括神经迁移和发育中的Lissencephaly基因(LIS1)。附属组织包括心脏和眼睛,相关表型为巨脑和全球发育延迟。
Related ID:
MALACARDS:HGJ001
OMIM:616355
MESH:D008607
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
未知
<1/1000000
10
52
12
HGJ001
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
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Gene
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Score
Mutations
No data available
Related Drugs
Name
CAS Number
Status
Phase
No data available
Disease Model
Category
Name
MGI
Related Gene
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Publications
No data available
References Literature
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PMID
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IF
No Data Found!
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