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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
Cornelia De Lange Syndrome (BDLS)
Alias:
Brachmann-De Lange Syndrome
De Lange Syndrome
Brachmann De Lange Syndrome
Cdls
Bdls
Typus Degenerativus Amstelodamensis
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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
科尼利亚·德·兰格综合症,也称为布拉赫曼-德·兰格综合症,与科尼利亚·德·兰格综合症1和科尼利亚·德·兰格综合症3有关,伴有或不伴有中线脑缺陷。与科尼利亚·德·兰格综合症相关的重要基因是NIPBL(NIPBL共着因子),其相关通路/超级通路包括细胞周期、有丝分裂和EML4和NUDC在有丝分裂纺锤体形成中的作用。在该疾病的背景下,已提到的药物有乙酰半胱氨酸和半胱氨酸。相关组织包括眼睛和骨骼,相关表型为智力障碍和高腭。
Related ID:
MALACARDS:CRN015
MESH:D003635
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
X显
常显
X染色体
胎儿期
1-9/1000000
85
568
112
CRN015
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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