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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
Kleefstra Syndrome 2 (KLEFS2)
Alias:
Klefs2
Kleefstra Syndrome, Type 2
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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
克利夫斯特拉综合症2,也称为klefs2,与克利夫斯特拉综合症和自闭症有关。与克利夫斯特拉综合症2有关的重要基因是KMT2C(赖氨酸甲基转移酶2C),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。附属组织包括眼睛和乳腺,相关表型为智力障碍和癫痫。
Related ID:
MALACARDS:KLF005
OMIM:617768
MESH:D065886
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
未知
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8
54
10
KLF005
Medical Symptom
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Gene & Mutation
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Publications
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