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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
Coffin-Siris Syndrome 4 (CSS4)
Alias:
Mrd16
Css4
Mental Retardation, Autosomal Dominant 16
Intellectual Disability, Autosomal Dominant 16
Autosomal Dominant Mental Retardation 16
Coffin-Siris Syndrome, Type 4
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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
Coffin-Siris Syndrome 4,也被称为mrd16,与Coffin-Siris Syndrome 1和挛缩、翼状胬肉和脊柱-掌骨-跖骨融合综合征1a有关。与Coffin-Siris Syndrome 4有关的重要基因是SMARCA4(SWI/SNF相关,矩阵相关,肌动蛋白依赖的染色质调节因子亚家族A,成员4),其相关通路/超通路包括RUNX1与作用于RUNX1靶点的精确效应尚不明确的共因子相互作用。相关组织包括心脏和骨骼,相关表型为智力障碍和全球发育延迟。
Related ID:
MALACARDS:CFF009
OMIM:614609
MESH:D000015
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
未知
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6
40
6
CFF009
Medical Symptom
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Categorization
Description
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Orphanet Frequency
HPO Source Accession
No data available
Gene & Mutation
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No data available
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Name
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No data available
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Category
Name
MGI
Related Gene
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